A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030998



Internal ID21940341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1656326..1666033hg38UCSC Ensembl
chr11:1677556..1687263hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg389708
hg199708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597064
Samples
Known GenesFAM99A, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030998
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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