A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588936



Internal ID20962007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78018575..78019318hg38UCSC Ensembl
chr11:77729621..77730364hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222251
Samples
Known GenesKCTD14, NDUFC2-KCTD14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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