A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146989



Internal ID346195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39973969..39974627hg38UCSC Ensembl
chr21:41345896..41346554hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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