A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269600



Internal ID20836640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29998549..30004205hg38UCSC Ensembl
chr5:29998656..30004312hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg385657
hg195657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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