A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557187



Internal ID330294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105196884..105197478hg38UCSC Ensembl
chr2:105813341..105813935hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16918631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557187
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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