A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957993



Internal ID16251949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3107884..3108657hg38UCSC Ensembl
Innerchr3:3149568..3150341hg19UCSC Ensembl
Innerchr3:3124568..3125341hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38774
hg19774
hg18774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589395
Supporting Variants
Samples
Known GenesIL5RA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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