A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573008



Internal ID20946079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23119090..23219502hg38UCSC Ensembl
chr8:22976603..23077015hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38100413
hg19100413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7300n223
Supporting Variantsnssv18277500
Samples
Known GenesTNFRSF10A, TNFRSF10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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