A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583292



Internal ID16370701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149507501..149544655hg38UCSC Ensembl
Innerchr2:150364015..150401169hg19UCSC Ensembl
Innerchr2:150072261..150109415hg18UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg3837155
hg1937155
hg1837155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv921245
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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