A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691075



Internal ID15081041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135714078..135789055hg38UCSC Ensembl
Innerchr9:138605924..138680901hg19UCSC Ensembl
Innerchr9:137745745..137820722hg18UCSC Ensembl
Innerchr9:135831869..135906846hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3874978
hg1974978
hg1874978
hg1774978
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517335
Supporting Variants
Samples
Known GenesKCNT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691075
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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