A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661508



Internal ID15051474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83611204..83640850hg38UCSC Ensembl
Innerchr9:86226119..86255765hg19UCSC Ensembl
Innerchr9:85415939..85445585hg18UCSC Ensembl
Innerchr9:83455673..83485319hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3829647
hg1929647
hg1829647
hg1729647
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516587
Supporting Variants
Samples
Known GenesIDNK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661508
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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