A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700329



Internal ID15436981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12234969..12239604hg38UCSC Ensembl
Innerchr9:12234969..12239604hg19UCSC Ensembl
Innerchr9:12224969..12229604hg18UCSC Ensembl
Innerchr9:12224969..12229604hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384636
hg194636
hg184636
hg174636
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700329
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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