A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970923



Internal ID22745858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149477281..149478461hg38UCSC Ensembl
chr5:148856844..148858024hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424908
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970923
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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