A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104172



Internal ID22013263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3256430..3273347hg38UCSC Ensembl
chr5:3256544..3273461hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3816918
hg1916918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104172
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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