A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583591



Internal ID16024314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:167180979..167276382hg38UCSC Ensembl
Innerchr2:168037489..168132892hg19UCSC Ensembl
Innerchr2:167745735..167841138hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3895404
hg1995404
hg1895404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv925270, nssv925269
Samples
Known GenesXIRP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583591
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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