A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979162



Internal ID53489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14818780..14820359hg38UCSC Ensembl
chr6:14819011..14820590hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467697
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979162
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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