A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429129



Internal ID207984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24673762..24674290hg38UCSC Ensembl
chr1:25000253..25000781hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429129
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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