A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639149



Internal ID18590744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:83955411..83984805hg38UCSC Ensembl
Innerchr5:83251230..83280624hg19UCSC Ensembl
Innerchr5:83286986..83316380hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3829395
hg1929395
hg1829395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017404
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)nssv3639149
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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