A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464987



Internal ID242858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3957770..3961363hg38UCSC Ensembl
chr6:3958004..3961597hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383594
hg193594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464987
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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