A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570902



Internal ID20943973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132628458..132629310hg38UCSC Ensembl
chr8:133640704..133641556hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277143
Samples
Known GenesLRRC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570902
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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