A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583168



Internal ID20956239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128570286..128571403hg38UCSC Ensembl
chr11:128440181..128441298hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381118
hg191118
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236717
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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