A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252046



Internal ID20819086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41742862..41837179hg38UCSC Ensembl
chr20:40371501..40465819hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3894318
hg1994319
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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