A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615927



Internal ID16056650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135714078..135738597hg38UCSC Ensembl
Innerchr9:138605924..138630443hg19UCSC Ensembl
Innerchr9:137745745..137770264hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3824520
hg1924520
hg1824520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148254
Samples
Known GenesKCNT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615927
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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