A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591112



Internal ID20964183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30327935..30328154hg38UCSC Ensembl
chr11:30349482..30349701hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232818
Samples
Known GenesARL14EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591112
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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