A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902313



Internal ID6264240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104165753..104365310hg19UCSC Ensembl
Outerchr14:104162263..104378087hg19UCSC Ensembl
Innerchr14:103235506..103435063hg18UCSC Ensembl
Outerchr14:103232016..103447840hg18UCSC 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 Variantsnssv1546857
SamplesMS17208
Known GenesKLC1, LOC145216, PPP1R13B, XRCC3, ZFYVE21
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902313
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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