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nsv1018322

  • Variant Calls:11
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63,892

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 544 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):10,466,868-10,530,759Question Mark
Overlapping variant regions from other studies: 219 SVs from 47 studies. See in: genome view    
Remapped(Score: Pass):1-41,643Question Mark
Overlapping variant regions from other studies: 544 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):10,467,101-10,530,992Question Mark
Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view    
Submitted genomic10,575,087-10,638,978Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1018322RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr610,466,86810,530,759
nsv1018322RemappedPassGRCh38.p12PATCHESSecond PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nsv1018322RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr610,467,10110,530,992
nsv1018322Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr610,575,08710,638,978

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3654767copy number lossSNP arrayProbe signal intensity
nssv3654768copy number lossSNP arrayProbe signal intensity
nssv3654769copy number lossSNP arrayProbe signal intensity
nssv3654770copy number lossSNP arrayProbe signal intensity
nssv3654771copy number lossSNP arrayProbe signal intensity
nssv3654772copy number lossSNP arrayProbe signal intensity
nssv3749021copy number lossSNP arrayProbe signal intensity
nssv3749022copy number lossSNP arrayProbe signal intensity
nssv3749023copy number lossSNP arrayProbe signal intensity
nssv3749024copy number lossSNP arrayProbe signal intensity
nssv3749025copy number lossSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3654767RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3654768RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3654769RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3654770RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3654771RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3654772RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3749021RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3749022RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3749023RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3749024RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3749025RemappedPassNW_018654713.1:g.(
?_1)_(41643_?)del
GRCh38.p12Second PassNW_018654713.1Chr6|NW_01
8654713.1
141,643
nssv3654767RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3654768RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3654769RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3654770RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3654771RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3654772RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3749021RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3749022RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3749023RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3749024RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3749025RemappedPerfectNC_000006.12:g.(?_
10466868)_(1053075
9_?)del
GRCh38.p12First PassNC_000006.12Chr610,466,86810,530,759
nssv3654767RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3654768RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3654769RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3654770RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3654771RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3654772RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3749021RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3749022RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3749023RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3749024RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3749025RemappedPerfectNC_000006.11:g.(?_
10467101)_(1053099
2_?)del
GRCh37.p13First PassNC_000006.11Chr610,467,10110,530,992
nssv3654767Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3654768Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3654769Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3654770Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3654771Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3654772Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3749021Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3749022Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3749023Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3749024Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978
nssv3749025Submitted genomicNC_000006.10:g.(?_
10575087)_(1063897
8_?)del
NCBI36 (hg18)NC_000006.10Chr610,575,08710,638,978

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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