U.S. flag

An official website of the United States government

nsv3918149

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:42,006,675
  • Description:GRCh38/hg38 3q25.31-29(chr3:156118441-198125115)x3 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 117244 SVs from 143 studies. See in: genome view    
Submitted genomic156,118,441-198,125,115Question Mark
Overlapping variant regions from other studies: 117243 SVs from 143 studies. See in: genome view    
Submitted genomic155,836,230-197,851,986Question Mark
Overlapping variant regions from other studies: 30737 SVs from 40 studies. See in: genome view    
Submitted genomic157,318,924-199,336,383Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeAssemblyAssembly UnitSequence IDChrInner StartInner Stop
nsv3918149Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3156,118,441198,125,115
nsv3918149Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3155,836,230197,851,986
nsv3918149Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr3157,318,924199,336,383

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15147555copy number gainMultipleMultipleSee casesPathogenicClinVarRCV000142310.5, VCV000154213.23

Variant Call Placement Information

Variant Call IDPlacement TypeHGVSAssemblySequence IDChrInner StartInner Stop
nssv15147555Submitted genomicNC_000003.12:g.(?_
156118441)_(198125
115_?)dup
GRCh38 (hg38)NC_000003.12Chr3156,118,441198,125,115
nssv15147555Submitted genomicNC_000003.11:g.(?_
155836230)_(197851
986_?)dup
GRCh37 (hg19)NC_000003.11Chr3155,836,230197,851,986
nssv15147555Submitted genomicNC_000003.10:g.(?_
157318924)_(199336
383_?)dup
NCBI36 (hg18)NC_000003.10Chr3157,318,924199,336,383

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15147555GRCh37: NC_000003.11:g.(?_155836230)_(197851986_?)dup, GRCh38: NC_000003.12:g.(?_156118441)_(198125115_?)dup, NCBI36: NC_000003.10:g.(?_157318924)_(199336383_?)dupcopy number gainnot providedSee casesPathogenicClinVarRCV000142310.5, VCV000154213.23

No genotype data were submitted for this variant

Support Center