A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567509



Internal ID20940580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34766275..34766810hg38UCSC Ensembl
chr8:34623793..34624328hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567509
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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