A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698808



Internal ID15435460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133255801..133255935hg38UCSC Ensembl
Innerchr9:136131188..136131322hg19UCSC Ensembl
Innerchr9:135121009..135121143hg18UCSC Ensembl
Innerchr9:133160742..133160876hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38135
hg19135
hg18135
hg17135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516103
Supporting Variants
Samples
Known GenesABO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698808
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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