A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721467



Internal ID18673062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25889808..25974422hg38UCSC Ensembl
Innerchr15:26134955..26219569hg19UCSC Ensembl
Innerchr15:23686048..23770662hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3884615
hg1984615
hg1884615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037821
Supporting Variants
Samples
Known GenesLOC100128714
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721467
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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