A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594049



Internal ID20967120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33647110..33648214hg38UCSC Ensembl
chr11:33668656..33669760hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223898
Samples
Known GenesKIAA1549L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594049
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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