A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583251



Internal ID16370660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:145962603..146022529hg38UCSC Ensembl
Innerchr2:146720171..146780097hg19UCSC Ensembl
Innerchr2:146436641..146496567hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3859927
hg1959927
hg1859927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7097n54
Supporting Variantsnssv920283
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583251
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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