A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440782



Internal ID219282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230781561..230783454hg38UCSC Ensembl
chr1:230917307..230919200hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381894
hg191894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16896891
Samples
Known GenesCAPN9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440782
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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