A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553869



Internal ID20926981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51546746..51548192hg38UCSC Ensembl
chr3:51580762..51582208hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg381447
hg191447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260794
Samples
Known GenesRAD54L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553869
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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