A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639150



Internal ID18590745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:83955411..83987123hg38UCSC Ensembl
Innerchr5:83251230..83282942hg19UCSC Ensembl
Innerchr5:83286986..83318698hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3831713
hg1931713
hg1831713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026174
Supporting Variants
Samples
Known GenesEDIL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639150
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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