A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581653



Internal ID16022376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43226244..43227591hg38UCSC Ensembl
Innerchr2:43453383..43454730hg19UCSC Ensembl
Innerchr2:43306887..43308234hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381348
hg191348
hg181348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6828n54
Supporting Variantsnssv907890
Samples
Known GenesLINC01126, ZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581653
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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