A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584704



Internal ID20957775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122939059..122940355hg38UCSC Ensembl
chr11:122809767..122811063hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381297
hg191297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234917
Samples
Known GenesC11orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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