A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137175



Internal ID20704215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116748521..116750510hg38UCSC Ensembl
chr6:117069684..117071673hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137175
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