A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087182



Internal ID21996415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73537821..73537821hg38UCSC Ensembl
chr11:73248866..73248866hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590437
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087182
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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