A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687772



Internal ID15077738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135667037..135803389hg38UCSC Ensembl
Innerchr9:138558883..138695235hg19UCSC Ensembl
Innerchr9:137698704..137835056hg18UCSC Ensembl
Innerchr9:135784828..135921180hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38136353
hg19136353
hg18136353
hg17136353
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517335
Supporting Variants
Samples
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687772
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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