A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569218



Internal ID20942289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126404000..126404381hg38UCSC Ensembl
chr8:127416245..127416626hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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