A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699628



Internal ID15436280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:30027282..30032966hg38UCSC Ensembl
Innerchr8:29884798..29890482hg19UCSC Ensembl
Innerchr8:30004340..30010024hg18UCSC Ensembl
Innerchr8:30004340..30010024hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385685
hg195685
hg185685
hg175685
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517326
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699628
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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