A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502053



Internal ID20875294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24620908..24675425hg38UCSC Ensembl
chr16:24632229..24686746hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3854518
hg1954518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502053
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