A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586076



Internal ID20959147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73587361..73587876hg38UCSC Ensembl
chr11:73298406..73298921hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220330
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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