A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432694



Internal ID211431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42690525..42690648hg38UCSC Ensembl
chr1:43156196..43156319hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16904854
Samples
Known GenesYBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432694
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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