A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902308



Internal ID6264235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104092789..104205811hg19UCSC Ensembl
Outerchr14:104087209..104211180hg19UCSC Ensembl
Innerchr14:103162542..103275564hg18UCSC Ensembl
Outerchr14:103156962..103280933hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1549864
SamplesMS18276
Known GenesKLC1, PPP1R13B, XRCC3, ZFYVE21
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902308
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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