A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542059



Internal ID20915328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56121837..56127861hg38UCSC Ensembl
chr1:56587509..56593533hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg386025
hg196025
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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