A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614959



Internal ID16402368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100998254..100999759hg38UCSC Ensembl
Innerchr9:103760536..103762041hg19UCSC Ensembl
Innerchr9:102800357..102801862hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381506
hg191506
hg181506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12810n54
Supporting Variantsnssv1140219
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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