A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv897623



Internal ID6304634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62453952..62598144hg19UCSC Ensembl
Outerchr11:62438819..62603916hg19UCSC Ensembl
Innerchr11:62210528..62354720hg18UCSC Ensembl
Outerchr11:62195395..62360492hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1576720
SamplesIS34235
Known GenesBSCL2, C11orf48, C11orf83, GNG3, HNRNPUL2, HNRNPUL2-BSCL2, LRRN4CL, NXF1, POLR2G, STX5, TAF6L, TMEM179B, TMEM223, TTC9C, UBXN1, WDR74, ZBTB3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv897623
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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