A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692732



Internal ID18991013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136838087hg38UCSC Ensembl
Innerchr8:137681619..137850330hg19UCSC Ensembl
Innerchr8:137750801..137919512hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38168712
hg19168712
hg18168712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029640
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)nssv3692732
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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