A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109742



Internal ID22018975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82968627..82987712hg38UCSC Ensembl
chr3:83017778..83036863hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3819086
hg1919086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109742
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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