A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974775



Internal ID22749710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43723943..43910582hg38UCSC Ensembl
chr5:43724045..43910684hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38186640
hg19186640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423377
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974775
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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