A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699204



Internal ID15435856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101900303..101903795hg38UCSC Ensembl
Innerchr9:104662585..104666077hg19UCSC Ensembl
Innerchr9:103702406..103705898hg18UCSC Ensembl
Innerchr9:101742140..101745632hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg383493
hg193493
hg183493
hg173493
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521116
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699204
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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