A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593474



Internal ID20966545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76648254..76652977hg38UCSC Ensembl
chr11:76359298..76364021hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384724
hg194724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593474
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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