A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538679



Internal ID20911993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108127731..108128212hg38UCSC Ensembl
chr1:108670353..108670834hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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