A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112357



Internal ID22021590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42997225..46288118hg38UCSC Ensembl
chr14:43466428..46757321hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg383290894
hg193290894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611184
Samples
Known GenesC14orf28, FAM179B, FANCM, FKBP3, FSCB, KLHL28, LINC00871, MIS18BP1, PRPF39, SNORD127
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112357
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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