A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970553



Internal ID22745488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31191076..31192017hg38UCSC Ensembl
chr5:31191183..31192124hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414474
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970553
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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