A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697890



Internal ID15434542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17424902..17454898hg38UCSC Ensembl
Innerchr8:17282411..17312407hg19UCSC Ensembl
Innerchr8:17326782..17356776hg18UCSC Ensembl
Innerchr8:17326782..17356776hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3829997
hg1929997
hg1829995
hg1729995
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516180
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697890
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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