A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696532



Internal ID15086498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112596769..112612873hg38UCSC Ensembl
Innerchr9:115359049..115375153hg19UCSC Ensembl
Innerchr9:114398870..114414974hg18UCSC Ensembl
Innerchr9:112438604..112454708hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3816105
hg1916105
hg1816105
hg1716105
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515899
Supporting Variants
Samples
Known GenesKIAA1958
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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