A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577100



Internal ID20950171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36107279..36108327hg38UCSC Ensembl
chr11:36128829..36129877hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228783
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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