A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594444



Internal ID20967515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113486856..113487169hg38UCSC Ensembl
chr11:113357578..113357891hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594444
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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