A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589849



Internal ID21781892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59209875..59209875hg38UCSC Ensembl
chr11:58977348..58977348hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080900
Supporting Variants
Samples
Known GenesMPEG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589849
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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