A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142265



Internal ID20709305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163593803..163611180hg38UCSC Ensembl
chr6:164014835..164032212hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3817378
hg1917378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613968
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142265
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