A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086583



Internal ID21995816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93744968..93744968hg38UCSC Ensembl
chr11:93478134..93478134hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593400
Samples
Known GenesC11orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086583
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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