A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556877



Internal ID20929948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23115135..23202352hg38UCSC Ensembl
chr8:22972648..23059865hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3887218
hg1987218
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7300n223
Supporting Variantsnssv18277499
Samples
Known GenesTNFRSF10A, TNFRSF10C, TNFRSF10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556877
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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