A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029481



Internal ID20596521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24692394..24716480hg38UCSC Ensembl
chr16:24703715..24727801hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3824087
hg1924087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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