A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615189



Internal ID16055912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111483503..111484126hg38UCSC Ensembl
Innerchr9:114245783..114246406hg19UCSC Ensembl
Innerchr9:113285604..113286227hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38624
hg19624
hg18624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12851n54
Supporting Variantsnssv1141232, nssv1141231
Samples
Known GenesKIAA0368
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615189
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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