A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240965



Internal ID20808005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10650174..10650908hg38UCSC Ensembl
chr17:10553491..10554225hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592797
Supporting Variants
Samples
Known GenesMYH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240965
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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