A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593181



Internal ID20966252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30401731..30402958hg38UCSC Ensembl
chr11:30423278..30424505hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218313
Samples
Known GenesMPPED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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