A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615146



Internal ID16402555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108564871..108589156hg38UCSC Ensembl
Innerchr9:111327151..111351436hg19UCSC Ensembl
Innerchr9:110366972..110391257hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3824286
hg1924286
hg1824286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141033
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615146
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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