A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000166



Internal ID16946432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:70122098..70164597hg38UCSC Ensembl
Outerchr16:70156001..70198500hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3842500
hg1942500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952048
Supporting Variants
SamplesBILGI_BIOE
Known GenesPDPR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000166
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