A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580167



Internal ID20953238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10782903..10783688hg38UCSC Ensembl
chr11:10804450..10805235hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv976n223
Supporting Variantsnssv18218387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580167
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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