A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557754



Internal ID20930825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23213488..23214307hg38UCSC Ensembl
chr8:23071001..23071820hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277505
Samples
Known GenesTNFRSF10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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