A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580767



Internal ID20953838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132705607..132706073hg38UCSC Ensembl
chr11:132575502..132575968hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228027
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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