A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146761



Internal ID345966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27769599..27771272hg38UCSC Ensembl
chr22:28165587..28167260hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381674
hg191674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728264
Samples
Known GenesMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146761
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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