A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578337



Internal ID21770380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36287118..36287477hg38UCSC Ensembl
chr11:36308668..36309027hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023385
Supporting Variants
Samples
Known GenesCOMMD9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578337
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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