A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613827



Internal ID16401236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23912011..23917930hg38UCSC Ensembl
Innerchr9:23912009..23917928hg19UCSC Ensembl
Innerchr9:23902009..23907928hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385920
hg195920
hg185920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131824
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613827
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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