A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559541



Internal ID20932612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42859450..42859716hg38UCSC Ensembl
chr8:42714593..42714859hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278064
Samples
Known GenesRNF170
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559541
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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