A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579662



Internal ID21771705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101041052..101041052hg38UCSC Ensembl
chr11:100911783..100911783hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085556
Supporting Variants
Samples
Known GenesPGR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579662
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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