A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420701



Internal ID199796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240976000..240981523hg38UCSC Ensembl
chr2:241915417..241920940hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg385524
hg195524
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420701
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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