A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704603



Internal ID15441255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:48856895..48867388hg38UCSC Ensembl
Innerchr8:49769454..49779947hg19UCSC Ensembl
Innerchr8:49932007..49942500hg18UCSC Ensembl
Innerchr8:49932007..49942500hg17UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3810494
hg1910494
hg1810494
hg1710494
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528067
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704603
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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