A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110197



Internal ID22019430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189196682..189200357hg38UCSC Ensembl
chr2:190061408..190065083hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg383676
hg193676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110197
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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