A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034838



Internal ID20601878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19858981..19861449hg38UCSC Ensembl
chr17:19762294..19764762hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382469
hg192469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499293
Supporting Variants
Samples
Known GenesULK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034838
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