A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502730



Internal ID20875978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89578068..89628894hg38UCSC Ensembl
chr16:89644476..89695302hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3850827
hg1950827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177776
Samples
Known GenesCPNE7, DPEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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