A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135403



Internal ID20702444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111284438..111290429hg38UCSC Ensembl
chr6:111605641..111611632hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385992
hg195992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604676
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135403
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