A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569610



Internal ID20942681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52709680..53007943hg38UCSC Ensembl
chr8:53622240..53920503hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38298264
hg19298264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278196
Samples
Known GenesNPBWR1, RB1CC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569610
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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