A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744494



Internal ID19042775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167886977..168066217hg38UCSC Ensembl
Innerchr4:168808128..168987368hg19UCSC Ensembl
Innerchr4:169044703..169223943hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38179241
hg19179241
hg18179241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030723
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)nssv3744494
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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