A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721682



Internal ID18673277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34520906hg38UCSC Ensembl
Innerchr15:34695310..34813107hg19UCSC Ensembl
Innerchr15:32482602..32600399hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38117798
hg19117798
hg18117798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052868
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721682
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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