A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107885



Internal ID22017120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144552939..147007131hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382454193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107885
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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