A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568495



Internal ID20941566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42851486..42852568hg38UCSC Ensembl
chr8:42706629..42707711hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278062
Samples
Known GenesRNF170
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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