A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589799



Internal ID20962870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101399299..101610889hg38UCSC Ensembl
chr11:101270030..101481620hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38211591
hg19211591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234234
Samples
Known GenesMIR3920, TRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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