A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702034



Internal ID15438686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20099578..20113378hg38UCSC Ensembl
Innerchr8:19957089..19970889hg19UCSC Ensembl
Innerchr8:20001369..20015169hg18UCSC Ensembl
Innerchr8:20001369..20015169hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3813801
hg1913801
hg1813801
hg1713801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525841
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702034
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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