A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574734



Internal ID20947805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93002176..93002277hg38UCSC Ensembl
chr8:94014404..94014505hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574734
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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