A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998086



Internal ID19192593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:29380978..29388679hg38UCSC Ensembl
Outerchr16:29392299..29400000hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387702
hg197702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153049
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998086
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer