A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242955



Internal ID20809995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40575530..40577396hg38UCSC Ensembl
chr17:38731782..38733648hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242955
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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