A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615918



Internal ID16403327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135698139..135736970hg38UCSC Ensembl
Innerchr9:138589985..138628816hg19UCSC Ensembl
Innerchr9:137729806..137768637hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3838832
hg1938832
hg1838832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148249
Samples
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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