A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638517



Internal ID18936798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2623490..2648402hg38UCSC Ensembl
Innerchr5:2623604..2648516hg19UCSC Ensembl
Innerchr5:2676604..2701516hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3824913
hg1924913
hg1824913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024927
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)nssv3638517
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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