A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701908



Internal ID15438560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110101478..110110675hg38UCSC Ensembl
Innerchr8:111113707..111122904hg19UCSC Ensembl
Innerchr8:111182883..111192080hg18UCSC Ensembl
Innerchr8:111182883..111192080hg17UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg389198
hg199198
hg189198
hg179198
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525742
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701908
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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