A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696114



Internal ID15432766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82776771..82785008hg38UCSC Ensembl
Innerchr9:85391686..85399923hg19UCSC Ensembl
Innerchr9:84581506..84589743hg18UCSC Ensembl
Innerchr9:82621240..82629477hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg388238
hg198238
hg188238
hg178238
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518664
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696114
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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