A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563642



Internal ID20936713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65338818..65339475hg38UCSC Ensembl
chr8:66251053..66251710hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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