A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244458



Internal ID20811498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32884754..32884836hg38UCSC Ensembl
chr17:31211772..31211854hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584358
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244458
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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