A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143017



Internal ID18903825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:41865073..41865174hg38UCSC Ensembl
Outerchr21:43285182..43285283hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979785
SamplesKWS2
Known GenesPRDM15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143017
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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