U.S. flag

An official website of the United States government

nsv3918564

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:67,953
  • Description:
    GRCh38/hg38 4p16.3(chr4:958677-1026629)x4 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 746 SVs from 68 studies. See in: genome view    
Submitted genomic958,677-1,026,629Question Mark
Overlapping variant regions from other studies: 746 SVs from 68 studies. See in: genome view    
Submitted genomic952,465-1,020,417Question Mark
Overlapping variant regions from other studies: 366 SVs from 19 studies. See in: genome view    
Submitted genomic942,465-1,010,417Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeAssemblyAssembly UnitSequence IDChrInner StartInner Stop
nsv3918564Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4958,6771,026,629
nsv3918564Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4952,4651,020,417
nsv3918564Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4942,4651,010,417

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15121305copy number gainMultipleMultipleSee casesBenignClinVarRCV000140384.3, VCV000151680.14

Variant Call Placement Information

Variant Call IDPlacement TypeHGVSAssemblySequence IDChrInner StartInner Stop
nssv15121305Submitted genomicNC_000004.12:g.(?_
958677)_(1026629_?
)dup
GRCh38 (hg38)NC_000004.12Chr4958,6771,026,629
nssv15121305Submitted genomicNC_000004.11:g.(?_
952465)_(1020417_?
)dup
GRCh37 (hg19)NC_000004.11Chr4952,4651,020,417
nssv15121305Submitted genomicNC_000004.10:g.(?_
942465)_(1010417_?
)dup
NCBI36 (hg18)NC_000004.10Chr4942,4651,010,417

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15121305GRCh37: NC_000004.11:g.(?_952465)_(1020417_?)dup, GRCh38: NC_000004.12:g.(?_958677)_(1026629_?)dup, NCBI36: NC_000004.10:g.(?_942465)_(1010417_?)dupcopy number gainnot providedSee casesBenignClinVarRCV000140384.3, VCV000151680.14

No genotype data were submitted for this variant

Support Center