A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146498



Internal ID345703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42004769..42005061hg38UCSC Ensembl
chr22:42400773..42401065hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729192
Samples
Known GenesWBP2NL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146498
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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