A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583096



Internal ID20956167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57694182..57695123hg38UCSC Ensembl
chr11:57461654..57462595hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220045
Samples
Known GenesZDHHC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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