A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112464



Internal ID22021697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60514788..60629416hg38UCSC Ensembl
chr18:58182021..58296649hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38114629
hg19114629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112464
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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