A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142856



Internal ID19273530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105015391..105015469hg38UCSC Ensembl
Outerchr14:105481728..105481806hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979318, nssv3963822
SamplesKWS2, KWS1
Known GenesCDCA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142856
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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