A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503745



Internal ID20877001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84698101..84700700hg38UCSC Ensembl
chr16:84731707..84734306hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181601
Samples
Known GenesUSP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503745
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