A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267457



Internal ID20834497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161622276..161622877hg38UCSC Ensembl
chr5:161049282..161049883hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267457
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00068


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