A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522747



Internal ID15450040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86584751..86605370hg38UCSC Ensembl
Innerchr14:87051095..87071714hg19UCSC Ensembl
Innerchr14:86120848..86141467hg18UCSC Ensembl
Innerchr14:86120848..86141467hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3820620
hg1920620
hg1820620
hg1720620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698382
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522747
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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