A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000084



Internal ID17293036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:32155980..32185379hg38UCSC Ensembl
Outerchr16:32167301..32196700hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3829400
hg1929400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953811
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000084
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