A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581484



Internal ID16022207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38572678..38647035hg38UCSC Ensembl
Innerchr2:38799820..38874177hg19UCSC Ensembl
Innerchr2:38653324..38727681hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3874358
hg1974358
hg1874358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6789n54
Supporting Variantsnssv906874
Samples
Known GenesHNRNPLL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581484
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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