A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416854



Internal ID22474724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175088415..175096995hg38UCSC Ensembl
chr5:174515418..174523998hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg388581
hg198581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975729
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416854
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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