A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690032



Internal ID18988313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136858422hg38UCSC Ensembl
Innerchr8:137687873..137870665hg19UCSC Ensembl
Innerchr8:137757055..137939847hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38182793
hg19182793
hg18182793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033514
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)nssv3690032
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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