A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139458



Internal ID20706498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134910061..134915426hg38UCSC Ensembl
chr6:135231199..135236564hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385366
hg195366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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