A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581410



Internal ID16368819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35620051..35855307hg38UCSC Ensembl
Innerchr2:35845117..36080373hg19UCSC Ensembl
Innerchr2:35698621..35933877hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38235257
hg19235257
hg18235257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6771n54
Supporting Variantsnssv1150716
Samples1780854061_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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