A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252604



Internal ID20819644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50658449..50666585hg38UCSC Ensembl
chr20:49274986..49283122hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg388137
hg198137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597968
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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