A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105134



Internal ID22014368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168354822..168360318hg38UCSC Ensembl
chr1:168324060..168329556hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg385497
hg195497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105134
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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