A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596282



Internal ID21788325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102601115..102601431hg38UCSC Ensembl
chr11:102471846..102472162hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026907
Supporting Variants
Samples
Known GenesMMP20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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