A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431322



Internal ID210102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145575370..145576906hg38UCSC Ensembl
chr1:146035585..146037135hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg381537
hg191551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890073
Samples
Known GenesLOC100288142, LOC101929780, NBPF10, NBPF11, NBPF24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431322
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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