A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952745



Internal ID16954932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:119041291..119047288hg38UCSC Ensembl
Outerchr11:118912001..118918000hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385998
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999629
SamplesBILGI_BIOE
Known GenesHYOU1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952745
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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