A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575813



Internal ID20948884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111788495..111789108hg38UCSC Ensembl
chr11:111659219..111659832hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219251
Samples
Known GenesALG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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