A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146025



Internal ID20713065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85137001..85146100hg38UCSC Ensembl
chr6:85846719..85855818hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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