A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745867



Internal ID19044148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:30291894..30431012hg38UCSC Ensembl
Innerchr5:30292001..30431119hg19UCSC Ensembl
Innerchr5:30327758..30466876hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38139119
hg19139119
hg18139119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019680
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)nssv3745867
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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