A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016667



Internal ID19105884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36448793..36464260hg38UCSC Ensembl
Innerchr5:36448895..36464362hg19UCSC Ensembl
Innerchr5:36484652..36500119hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3815468
hg1915468
hg1815468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5631n100
Supporting Variantsnssv3637073
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)nsv1016667
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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