A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431091



Internal ID209876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145464587..145496587hg38UCSC Ensembl
chr1:145968239..146000214hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3832001
hg1931976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890056
Samples
Known GenesLOC100288142, LOC101929780, NBPF10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431091
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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