A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139559



Internal ID20706599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124909149..124913216hg38UCSC Ensembl
chr6:125230295..125234362hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384068
hg194068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611343
Supporting Variants
Samples
Known GenesSTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139559
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