A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100528



Internal ID22009761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108436085..108439873hg38UCSC Ensembl
chr12:108829862..108833650hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg383789
hg193789
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100528
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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