A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538883



Internal ID20912190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239288619..239291231hg38UCSC Ensembl
chr1:239451919..239454531hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg382613
hg192613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538883
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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