A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581652



Internal ID16022375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43226069..43227253hg38UCSC Ensembl
Innerchr2:43453208..43454392hg19UCSC Ensembl
Innerchr2:43306712..43307896hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381185
hg191185
hg181185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6828n54
Supporting Variantsnssv907889
Samples
Known GenesLINC01126, ZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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