A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984055



Internal ID56746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68654631..68705323hg38UCSC Ensembl
chr6:69364523..69415215hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3850693
hg1950693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471453
Supporting Variants
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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