A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578358



Internal ID20951429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86633846..86633934hg38UCSC Ensembl
chr11:86344888..86344976hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217744
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578358
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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