A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580501



Internal ID20953572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27747107..27747817hg38UCSC Ensembl
chr11:27768654..27769364hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580501
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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