A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638063



Internal ID18936344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99433955..99566850hg38UCSC Ensembl
Innerchr5:98769659..98902554hg19UCSC Ensembl
Innerchr5:98797558..98930453hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38132896
hg19132896
hg18132896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033351
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)nssv3638063
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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