A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961899



Internal ID19216529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:65865471..65865551hg38UCSC Ensembl
Outerchr16:65899374..65899454hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120329
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961899
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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