A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107570



Internal ID22016803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181103495..181183021hg38UCSC Ensembl
chr5:180530495..180610021hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3879527
hg1979527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564951
Samples
Known GenesOR2V1, OR2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107570
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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