A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559163



Internal ID20932234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94570703..94571579hg38UCSC Ensembl
chr8:95582931..95583807hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559163
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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