A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560428



Internal ID333435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231594858..231597835hg38UCSC Ensembl
chr2:232459569..232462546hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg382978
hg192978
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16926967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560428
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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