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nsv526224

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:66,835

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 161 SVs from 36 studies. See in: genome view    
Remapped(Score: Good):151,003,841-151,070,675Question Mark
Overlapping variant regions from other studies: 161 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):150,383,403-150,450,236Question Mark
Overlapping variant regions from other studies: 8 SVs from 3 studies. See in: genome view    
Submitted genomic150,363,596-150,430,429Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv526224RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5151,003,841151,070,675
nsv526224RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5150,383,403150,450,236
nsv526224Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000005.8Chr5150,363,596150,430,429

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv702490copy number gainSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv702490RemappedGoodNC_000005.10:g.(?_
151003841)_(151070
675_?)dup
GRCh38.p12First PassNC_000005.10Chr5151,003,841151,070,675
nssv702490RemappedPerfectNC_000005.9:g.(?_1
50383403)_(1504502
36_?)dup
GRCh37.p13First PassNC_000005.9Chr5150,383,403150,450,236
nssv702490Submitted genomicNC_000005.8:g.(?_1
50363596)_(1504304
29_?)dup
NCBI35 (hg17)NC_000005.8Chr5150,363,596150,430,429

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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