A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613831



Internal ID16401240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24125020..24154730hg38UCSC Ensembl
Innerchr9:24125018..24154728hg19UCSC Ensembl
Innerchr9:24115018..24144728hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3829711
hg1929711
hg1829711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131828, nssv1131829
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613831
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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