A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463614



Internal ID241512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125594959..125598925hg38UCSC Ensembl
chr6:125916105..125920071hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383967
hg193967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463614
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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