A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537190



Internal ID20910529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21085752..21086676hg38UCSC Ensembl
chr1:21412245..21413169hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247872
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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