A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951272



Internal ID16953459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:751201..911500hg38UCSC Ensembl
Outerchr11:751201..911500hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38160300
hg19160300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998114
SamplesBILGI_BIOE
Known GenesCD151, CEND1, CHID1, EFCAB4A, NS3BP, PDDC1, PIDD, PNPLA2, POLR2L, RPLP2, SLC25A22, SNORA52, TALDO1, TSPAN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951272
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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