A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581176



Internal ID20954247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66135014..66135956hg38UCSC Ensembl
chr11:65902485..65903427hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230273
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581176
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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