A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744489



Internal ID19042770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166393869..166482083hg38UCSC Ensembl
Innerchr4:167315021..167403235hg19UCSC Ensembl
Innerchr4:167534471..167622685hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3888215
hg1988215
hg1888215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028788
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)nssv3744489
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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