A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267679



Internal ID20476897
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 StatusS
Merged Variantsnsv4767466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267679
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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