A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278749



Internal ID20845789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77386605..77388050hg38UCSC Ensembl
chr8:78298841..78300286hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278749
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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