A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv914701



Internal ID15861971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102206419..102249813hg38UCSC Ensembl
Innerchr2:102822879..102866273hg19UCSC Ensembl
Innerchr2:102189311..102232705hg18UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3843395
hg1943395
hg1843395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582555
Supporting Variants
Samples
Known GenesIL1RL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv914701
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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