A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582821



Internal ID20955892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47709028..47709619hg38UCSC Ensembl
chr11:47730580..47731171hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218375
Samples
Known GenesAGBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582821
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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