A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419335



Internal ID22477205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8260597..8263756hg38UCSC Ensembl
chr5:8260710..8263869hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg383160
hg193160
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419335
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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