A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581642



Internal ID16369051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42231500..42304011hg38UCSC Ensembl
Innerchr2:42458640..42531151hg19UCSC Ensembl
Innerchr2:42312144..42384655hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3872512
hg1972512
hg1872512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907880
Samples
Known GenesEML4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581642
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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