A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578921



Internal ID20951992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57748093..57748426hg38UCSC Ensembl
chr11:57515565..57515898hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231943
Samples
Known GenesBTBD18, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578921
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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