A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538561



Internal ID20911875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204539193..204540245hg38UCSC Ensembl
chr1:204508321..204509373hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381053
hg191053
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249955
Samples
Known GenesMDM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538561
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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