A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673522



Internal ID15410174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2182928..2223287hg38UCSC Ensembl
Innerchr8:2131125..2170955hg19UCSC Ensembl
Innerchr8:2118532..2158362hg18UCSC Ensembl
Innerchr8:2118532..2158362hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3840360
hg1939831
hg1839831
hg1739831
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515930
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673522
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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