A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459622



Internal ID237634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48817175..48817564hg38UCSC Ensembl
chr6:48784812..48785201hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459622
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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