A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614151



Internal ID16401560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33635166..33666011hg38UCSC Ensembl
Innerchr9:33635164..33666009hg19UCSC Ensembl
Innerchr9:33625164..33656009hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3830846
hg1930846
hg1830846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132843
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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