A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765002



Internal ID20540862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12831453..12867129hg38UCSC Ensembl
chr2:12971579..13007255hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3835677
hg1935677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765002
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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