A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583186



Internal ID16370595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:139910635..139966125hg38UCSC Ensembl
Innerchr2:140668204..140723694hg19UCSC Ensembl
Innerchr2:140384674..140440164hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3855491
hg1955491
hg1855491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv920110
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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