A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468813



Internal ID246604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110309619..110340055hg38UCSC Ensembl
chr6:110630822..110661258hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3830437
hg1930437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987956
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468813
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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