A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988656



Internal ID20555696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18573781..18574977hg38UCSC Ensembl
chr11:18595328..18596524hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450281
Supporting Variants
Samples
Known GenesUEVLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988656
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