A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505384



Internal ID20878653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2463611..2466619hg38UCSC Ensembl
chr16:2513612..2516620hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383009
hg193009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029475
Samples
Known GenesC16orf59, MIR6768
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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