A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745742



Internal ID19044023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:13467778..13518647hg38UCSC Ensembl
Innerchr5:13467888..13518757hg19UCSC Ensembl
Innerchr5:13520888..13571757hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3850870
hg1950870
hg1850870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028943
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)nssv3745742
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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