A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538831



Internal ID20912145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7928885..7929444hg38UCSC Ensembl
chr1:7988945..7989504hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253200
Samples
Known GenesTNFRSF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538831
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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