A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427318



Internal ID22485188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142060496..142106228hg38UCSC Ensembl
chr5:141440061..141485793hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3845733
hg1945733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427318
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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