A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661262



Internal ID15051228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135667037..135789055hg38UCSC Ensembl
Innerchr9:138558883..138680901hg19UCSC Ensembl
Innerchr9:137698704..137820722hg18UCSC Ensembl
Innerchr9:135784828..135906846hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38122019
hg19122019
hg18122019
hg17122019
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517335
Supporting Variants
Samples
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661262
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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