A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577191



Internal ID20950262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118393135..118393599hg38UCSC Ensembl
chr11:118263850..118264314hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218220
Samples
Known GenesLOC100131626, UBE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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