A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564360



Internal ID20937431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125094862..125095598hg38UCSC Ensembl
chr8:126107104..126107840hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276172
Samples
Known GenesNSMCE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564360
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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