A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527140



Internal ID15454433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45279043..45314343hg38UCSC Ensembl
Innerchr14:45748246..45783546hg19UCSC Ensembl
Innerchr14:44817996..44853296hg18UCSC Ensembl
Innerchr14:44817996..44853296hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3835301
hg1935301
hg1835301
hg1735301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703528
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527140
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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