A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423684



Internal ID202698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:261666..287666hg38UCSC Ensembl
chr1:231417..257417hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3826001
hg1926001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16907125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423684
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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