A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689600



Internal ID18987881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83108669..83216385hg38UCSC Ensembl
Innerchr8:84020904..84128620hg19UCSC Ensembl
Innerchr8:84183459..84291175hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38107717
hg19107717
hg18107717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029506
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)nssv3689600
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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