A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979660



Internal ID18887077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88916234..88916312hg38UCSC Ensembl
Outerchr16:88982642..88982720hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142208
Supporting Variants
SamplesKWS2
Known GenesCBFA2T3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979660
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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