A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013843



Internal ID18756375
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 StatusM
Merged Variants
Supporting Variantsnssv3590382, nssv3739547
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)nsv1013843
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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