A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578548



Internal ID20951619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128535351..128537709hg38UCSC Ensembl
chr11:128405246..128407604hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382359
hg192359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232094
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578548
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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