A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288955



Internal ID20498173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12830476..12851567hg38UCSC Ensembl
chr2:12970602..12991693hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3821092
hg1921092
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752480
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288955
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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