A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538721



Internal ID20912035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154090705..154091320hg38UCSC Ensembl
chr1:154063181..154063796hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247072
Samples
Known GenesNUP210L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538721
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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