A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582537



Internal ID16369946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:101612166..101616867hg38UCSC Ensembl
Innerchr2:102228628..102233329hg19UCSC Ensembl
Innerchr2:101595060..101599761hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg384702
hg194702
hg184702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6977n54
Supporting Variantsnssv914559
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582537
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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