A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526831



Internal ID15454124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36408496..36419362hg38UCSC Ensembl
Innerchr14:36877701..36888567hg19UCSC Ensembl
Innerchr14:35947452..35958318hg18UCSC Ensembl
Innerchr14:35947452..35958318hg17UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3810867
hg1910867
hg1810867
hg1710867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv132n21
Supporting Variantsnssv703188
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526831
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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