A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541927



Internal ID20915195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12116680..12117083hg38UCSC Ensembl
chr1:12176737..12177140hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249901
Samples
Known GenesTNFRSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541927
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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