A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416158



Internal ID22474028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155906898..156286833hg38UCSC Ensembl
chr5:155333908..155713843hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38379936
hg19379936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416158
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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