A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244660



Internal ID20811700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5312986..5314102hg38UCSC Ensembl
chr18:5312985..5314101hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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