A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422609



Internal ID201650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91041068..91046868hg38UCSC Ensembl
chr1:91506625..91512425hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422609
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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