A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979322



Internal ID18883673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105439155..105439234hg38UCSC Ensembl
Outerchr14:105905492..105905571hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125600
Supporting Variants
SamplesKWS2
Known GenesMTA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979322
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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