A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703394



Internal ID15440046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14592182..14594503hg38UCSC Ensembl
Innerchr9:14592180..14594501hg19UCSC Ensembl
Innerchr9:14582180..14584501hg18UCSC Ensembl
Innerchr9:14582180..14584501hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382322
hg192322
hg182322
hg172322
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703394
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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