A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688828



Internal ID15078794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135724120..135752357hg38UCSC Ensembl
Innerchr9:138615966..138644203hg19UCSC Ensembl
Innerchr9:137755787..137784024hg18UCSC Ensembl
Innerchr9:135841911..135870148hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3828238
hg1928238
hg1828238
hg1728238
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)nssv688828
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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