A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252029



Internal ID20819069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40259616..40260708hg38UCSC Ensembl
chr20:38888256..38889348hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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