A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109142



Internal ID22018375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103514059..103529113hg38UCSC Ensembl
chr1:104056681..104071735hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3815055
hg1915055
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521828
Samples
Known GenesLOC101928436, RNPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109142
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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