A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584042



Internal ID16371451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:187814246..187928511hg38UCSC Ensembl
Innerchr2:188678973..188793238hg19UCSC Ensembl
Innerchr2:188387218..188501483hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38114266
hg19114266
hg18114266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151343
Samples1780854536_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584042
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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