A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689997



Internal ID18988278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136854535hg38UCSC Ensembl
Innerchr8:137681619..137866778hg19UCSC Ensembl
Innerchr8:137750801..137935960hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38185160
hg19185160
hg18185160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024457
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)nssv3689997
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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