A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589501



Internal ID20962572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63600857..63602023hg38UCSC Ensembl
chr11:63368329..63369495hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219213
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589501
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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