A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108657



Internal ID22017890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98953079..98954787hg38UCSC Ensembl
chr1:99418635..99420343hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381709
hg191709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522535
Samples
Known GenesLPPR5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108657
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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