A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440522



Internal ID219024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213411836..213414116hg38UCSC Ensembl
chr1:213585179..213587459hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg382281
hg192281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16896136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440522
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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