A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583589



Internal ID16370998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:167167818..167217320hg38UCSC Ensembl
Innerchr2:168024328..168073830hg19UCSC Ensembl
Innerchr2:167732574..167782076hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3849503
hg1949503
hg1849503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7156n54
Supporting Variantsnssv925267
Samples
Known GenesXIRP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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