A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555938



Internal ID20929009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24410130..24410950hg38UCSC Ensembl
chr6:24410358..24411178hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270856
Samples
Known GenesMRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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