A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242518



Internal ID20809558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48447544..48448486hg38UCSC Ensembl
chr17:46524906..46525848hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242518
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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