A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904891



Internal ID15852161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33047387..33076880hg38UCSC Ensembl
Innerchr2:33272454..33301947hg19UCSC Ensembl
Innerchr2:33125958..33155451hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3829494
hg1929494
hg1829494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581309
Supporting Variants
Samples
Known GenesLTBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904891
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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