A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615920



Internal ID16403329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135698139..135761806hg38UCSC Ensembl
Innerchr9:138589985..138653652hg19UCSC Ensembl
Innerchr9:137729806..137793473hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3863668
hg1963668
hg1863668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12993n54
Supporting Variantsnssv1176012
SamplesNINDS_60
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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