A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988030



Internal ID18876326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:122863258..122863382hg38UCSC Ensembl
Outerchr11:122733966..122734090hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133175
Supporting Variants
SamplesKWS1
Known GenesCRTAM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988030
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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