A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613685



Internal ID16401094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16884295..16887075hg38UCSC Ensembl
Innerchr9:16884293..16887073hg19UCSC Ensembl
Innerchr9:16874293..16877073hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg382781
hg192781
hg182781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129317
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613685
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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