A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998018



Internal ID19191248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:63120295..63128096hg38UCSC Ensembl
Outerchr16:63154199..63162000hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387802
hg197802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152981
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998018
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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