A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969023



Internal ID46675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124890320..124905180hg38UCSC Ensembl
chr6:125211466..125226326hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3814861
hg1914861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969023
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001562


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