A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278269



Internal ID20845309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55532769..55534453hg38UCSC Ensembl
chr8:56445328..56447012hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381685
hg191685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568551
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278269
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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