A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639185



Internal ID18937466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:89909931..89945661hg38UCSC Ensembl
Innerchr5:89205748..89241478hg19UCSC Ensembl
Innerchr5:89241504..89277234hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3835731
hg1935731
hg1835731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029685
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639185
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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