A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278400



Internal ID20845440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61992971..62239354hg38UCSC Ensembl
chr8:62905530..63151913hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38246384
hg19246384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278400
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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