A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566494



Internal ID20939565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138283825..138284867hg38UCSC Ensembl
chr8:139296068..139297110hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7523n223
Supporting Variantsnssv18277223
Samples
Known GenesFAM135B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566494
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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