A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588812



Internal ID20961883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47831683..47832008hg38UCSC Ensembl
chr11:47853235..47853560hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234194
Samples
Known GenesNUP160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588812
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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