A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584232



Internal ID20957303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59605041..59605676hg38UCSC Ensembl
chr11:59372514..59373149hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221033
Samples
Known GenesOSBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584232
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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