A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582469



Internal ID20955540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73795260..73796796hg38UCSC Ensembl
chr11:73506305..73507841hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221683
Samples
Known GenesMRPL48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582469
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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