A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988105



Internal ID18877296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:8562985..8563144hg38UCSC Ensembl
Outerchr16:8612987..8613146hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133222
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988105
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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