A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053462



Internal ID18795993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40977869..41103896hg38UCSC Ensembl
Innerchr15:41270067..41396094hg19UCSC Ensembl
Innerchr15:39057359..39183386hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38126028
hg19126028
hg18126028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552252
Samples
Known GenesINO80
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053462
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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