A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977921



Internal ID52682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80000..1240000hg38UCSC Ensembl
chr6:80000..1240235hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381160001
hg191160236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460400
Supporting Variants
Samples
Known GenesDUSP22, EXOC2, HUS1B, IRF4, LOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977921
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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