A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578456



Internal ID21770499
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 StatusS
Merged Variantsnsv6087573
Supporting Variants
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578456
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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