A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698828



Internal ID15435480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106805428..106810920hg38UCSC Ensembl
Innerchr8:107817656..107823148hg19UCSC Ensembl
Innerchr8:107886832..107892324hg18UCSC Ensembl
Innerchr8:107886832..107892324hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg385493
hg195493
hg185493
hg175493
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523126
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698828
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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