A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252629



Internal ID20819669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51352254..51352637hg38UCSC Ensembl
chr20:49968791..49969174hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598537
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252629
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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