A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976465



Internal ID22751400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86348572..86348740hg38UCSC Ensembl
chr1:86814255..86814423hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371236
Samples
Known GenesODF2L
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976465
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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