A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585972



Internal ID21778015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14879591..14879709hg38UCSC Ensembl
chr11:14901137..14901255hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036264
Supporting Variants
Samples
Known GenesCYP2R1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585972
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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