A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902300



Internal ID6264227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103979953..104198251hg19UCSC Ensembl
Outerchr14:103967504..104205811hg19UCSC Ensembl
Innerchr14:103049706..103268004hg18UCSC Ensembl
Outerchr14:103037257..103275564hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1580899
SamplesIS35484
Known GenesAPOPT1, BAG5, CKB, KLC1, MARK3, PPP1R13B, TRMT61A, XRCC3, ZFYVE21
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902300
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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