A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593271



Internal ID20966342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66702367..66702810hg38UCSC Ensembl
chr11:66469838..66470281hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223668
Samples
Known GenesSPTBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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