A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979575



Internal ID18899921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125425821..125425915hg38UCSC Ensembl
Outerchr11:125295717..125295811hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140493
Supporting Variants
SamplesKWS2
Known GenesPKNOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979575
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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