A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614786



Internal ID16402195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87307712..87308356hg38UCSC Ensembl
Innerchr9:89922627..89923271hg19UCSC Ensembl
Innerchr9:89112447..89113091hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38645
hg19645
hg18645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139084
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614786
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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