A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027536



Internal ID21936879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111692999..111698325hg38UCSC Ensembl
chr11:111563723..111569049hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg385327
hg195327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608724
Samples
Known GenesSIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027536
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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