A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581514



Internal ID20954585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59583157..59583634hg38UCSC Ensembl
chr11:59350630..59351107hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228880
Samples
Known GenesOSBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581514
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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