A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615915



Internal ID16056638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135667116..135703595hg38UCSC Ensembl
Innerchr9:138558962..138595441hg19UCSC Ensembl
Innerchr9:137698783..137735262hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3836480
hg1936480
hg1836480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12990n54
Supporting Variantsnssv1148245
Samples
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615915
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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