A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986057



Internal ID58125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63784659..63787191hg38UCSC Ensembl
chr6:64494552..64497084hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382533
hg192533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466253
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986057
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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