A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760503



Internal ID18712098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38199815..38310837hg38UCSC Ensembl
Innerchr8:38057333..38168355hg19UCSC Ensembl
Innerchr8:38176490..38287512hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38111023
hg19111023
hg18111023
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016632
Supporting Variants
Samples
Known GenesBAG4, DDHD2, PPAPDC1B, WHSC1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760503
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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