A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106881



Internal ID22016114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170170464..170171751hg38UCSC Ensembl
chr5:169597468..169598755hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381288
hg191288
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106881
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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