A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615919



Internal ID16403328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135698139..135746536hg38UCSC Ensembl
Innerchr9:138589985..138638382hg19UCSC Ensembl
Innerchr9:137729806..137778203hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3848398
hg1948398
hg1848398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12991n54
Supporting Variantsnssv1176011
SamplesHGDP01351
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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