A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980891



Internal ID19203573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:119363790..119364590hg38UCSC Ensembl
Outerchr11:119234500..119235300hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118222
Supporting Variants
SamplesKWS1
Known GenesUSP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980891
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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