A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429744



Internal ID208581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165777625..165778197hg38UCSC Ensembl
chr1:165746862..165747434hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429744
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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