A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682102



Internal ID15072068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135711894..135746536hg38UCSC Ensembl
Innerchr9:138603740..138638382hg19UCSC Ensembl
Innerchr9:137743561..137778203hg18UCSC Ensembl
Innerchr9:135829685..135864327hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3834643
hg1934643
hg1834643
hg1734643
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)nssv682102
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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