A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591179



Internal ID20964250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73777516..73778347hg38UCSC Ensembl
chr11:73488561..73489392hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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