A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746162



Internal ID18697757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:4980866..5391118hg38UCSC Ensembl
Innerchr5:4980979..5391231hg19UCSC Ensembl
Innerchr5:5033979..5444231hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38410253
hg19410253
hg18410253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024784
Supporting Variants
Samples
Known GenesADAMTS16, LINC01020
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746162
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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