A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593523



Internal ID20966594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9449472..9449823hg38UCSC Ensembl
chr11:9471019..9471370hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593523
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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