A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568603



Internal ID20941674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115064082..115064661hg38UCSC Ensembl
chr8:116076311..116076890hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7472n223
Supporting Variantsnssv18277003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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