A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591675



Internal ID20964746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76397900..76398604hg38UCSC Ensembl
chr11:76108944..76109648hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1231n223
Supporting Variantsnssv18217272
Samples
Known GenesLOC100506127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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