A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456775



Internal ID234835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125336268..125339807hg38UCSC Ensembl
chr6:125657414..125660953hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383540
hg193540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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