A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578912



Internal ID20951983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122970062..122970182hg38UCSC Ensembl
chr11:122840770..122840890hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578912
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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