A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999620



Internal ID16945886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:114058779..114061778hg38UCSC Ensembl
Outerchr11:113929501..113932500hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952735
Supporting Variants
SamplesBILGI_BIOE
Known GenesZBTB16
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999620
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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