A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987398



Internal ID59040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79177897..79181729hg38UCSC Ensembl
chr6:79887614..79891446hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383833
hg193833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003592


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