A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579003



Internal ID20952074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114349791..114354247hg38UCSC Ensembl
chr11:114220513..114224969hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg384457
hg194457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579003
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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