A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635869



Internal ID18934150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18607196..18664975hg38UCSC Ensembl
Innerchr5:18607305..18665084hg19UCSC Ensembl
Innerchr5:18643062..18700841hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3857780
hg1957780
hg1857780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027642
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)nssv3635869
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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