A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585558



Internal ID20958629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124484680..124485367hg38UCSC Ensembl
chr11:124354576..124355263hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585558
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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