A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582358



Internal ID16369767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:83000131..83123080hg38UCSC Ensembl
Innerchr2:83227255..83350204hg19UCSC Ensembl
Innerchr2:83080766..83203715hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38122950
hg19122950
hg18122950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6944n54
Supporting Variantsnssv1150778, nssv1150779, nssv1150777, nssv1150780
Samples1780862042_A, 1780854261_A, 1782681317_A, 1780862432_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582358
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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