A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713776



Internal ID19012057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20406244hg38UCSC Ensembl
Innerchr15:20564575..20611497hg19UCSC Ensembl
Innerchr15:18824589..18871511hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3846923
hg1946923
hg1846923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054141
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713776
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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