A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463071



Internal ID240987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122207884..122208003hg38UCSC Ensembl
chr6:122529030..122529149hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463071
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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