A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596104



Internal ID21788147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18561789..18561857hg38UCSC Ensembl
chr11:18583336..18583404hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039118
Supporting Variants
Samples
Known GenesUEVLD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596104
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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