A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553923



Internal ID20927033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40224307..40225614hg38UCSC Ensembl
chr1:40689979..40691286hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250924
Samples
Known GenesRLF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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