A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660069



Internal ID15050035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135711894..135736970hg38UCSC Ensembl
Innerchr9:138603740..138628816hg19UCSC Ensembl
Innerchr9:137743561..137768637hg18UCSC Ensembl
Innerchr9:135829685..135854761hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3825077
hg1925077
hg1825077
hg1725077
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)nssv660069
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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