A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970545



Internal ID47689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144864050..145013145hg38UCSC Ensembl
chr6:145185186..145334281hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38149096
hg19149096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970545
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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