A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv897797



Internal ID6304808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67024534..67288594hg19UCSC Ensembl
Outerchr11:67023040..67293234hg19UCSC Ensembl
Innerchr11:66781110..67045170hg18UCSC Ensembl
Outerchr11:66779616..67049810hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510028
SamplesSP54956
Known GenesADRBK1, AIP, ANKRD13D, CABP2, CABP4, CARNS1, CDK2AP2, CLCF1, CORO1B, GPR152, KDM2A, LOC100130987, PITPNM1, POLD4, PPP1CA, PTPRCAP, RAD9A, RPS6KB2, SSH3, TBC1D10C, TMEM134
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv897797
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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