A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579759



Internal ID20952830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118538195..118538897hg38UCSC Ensembl
chr11:118408910..118409612hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225454
Samples
Known GenesTMEM25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579759
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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