A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614312



Internal ID16401721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62094968..62098635hg38UCSC Ensembl
Innerchr9:40228872..40232540hg19UCSC Ensembl
Innerchr9:40218872..40222540hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383668
hg193669
hg183669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12696n54
Supporting Variantsnssv1134132
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614312
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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