A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590382



Internal ID18541977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3058965..3088961hg38UCSC Ensembl
Innerchr3:3100649..3130645hg19UCSC Ensembl
Innerchr3:3075649..3105645hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3829997
hg1929997
hg1829997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013843
Supporting Variants
Samples
Known GenesIL5RA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590382
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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