A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107513



Internal ID22016746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120818947..120819174hg38UCSC Ensembl
chr3:120537794..120538021hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107513
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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