A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613743



Internal ID16401152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20203729..20282324hg38UCSC Ensembl
Innerchr9:20203727..20282322hg19UCSC Ensembl
Innerchr9:20193727..20272322hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3878596
hg1978596
hg1878596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130793
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613743
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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