A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498832



Internal ID20872045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87406031..87425540hg38UCSC Ensembl
chr16:87439637..87459146hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3819510
hg1919510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187389
Samples
Known GenesZCCHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498832
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