A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613134



Internal ID16400543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2424322..2466509hg38UCSC Ensembl
Innerchr9:2424322..2466509hg19UCSC Ensembl
Innerchr9:2414322..2456509hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3842188
hg1942188
hg1842188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126218
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613134
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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