A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767466



Internal ID20543326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89002427..90228531hg38UCSC Ensembl
chr2:89301924..90267397hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381226105
hg19965474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767466
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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