A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424829



Internal ID22482699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116715795..116716653hg38UCSC Ensembl
chr5:116051491..116052349hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969272
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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