A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691528



Internal ID18989809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131058619..131182861hg38UCSC Ensembl
Innerchr8:132070866..132195108hg19UCSC Ensembl
Innerchr8:132140048..132264290hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38124243
hg19124243
hg18124243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030858
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)nssv3691528
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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