A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414263



Internal ID193546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90869295..90877470hg38UCSC Ensembl
chr1:91334852..91343027hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg388176
hg198176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414263
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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