A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536937



Internal ID18835218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20422227hg38UCSC Ensembl
Innerchr15:20216943..20627480hg19UCSC Ensembl
Innerchr15:18476957..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38410538
hg19410538
hg18410538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035246
Supporting Variants
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536937
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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