A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102457



Internal ID22011692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79260363..79451468hg38UCSC Ensembl
chr2:79487489..79678594hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38191106
hg19191106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102457
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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