A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581154



Internal ID16368563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:19774936..19795709hg38UCSC Ensembl
Innerchr2:19974697..19995470hg19UCSC Ensembl
Innerchr2:19838178..19858951hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3820774
hg1920774
hg1820774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150408
SamplesHGDP00830
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581154
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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