A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620595



Internal ID18572190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24596770..24690264hg38UCSC Ensembl
Innerchr4:24598393..24691887hg19UCSC Ensembl
Innerchr4:24207491..24300985hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3893495
hg1993495
hg1893495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011284
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)nssv3620595
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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