A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580032



Internal ID20953103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78115459..78116438hg38UCSC Ensembl
chr11:77826505..77827484hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38980
hg19980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218407
Samples
Known GenesALG8, RNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580032
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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