A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087573



Internal ID21996806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78742366..78742366hg38UCSC Ensembl
chr11:78453411..78453411hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578456
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087573
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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