A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110152



Internal ID21293418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:40569394..40579519hg38UCSC Ensembl
Innerchr21:41941321..41951446hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3810126
hg1910126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101974
Samplessample165
Known GenesDSCAM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110152
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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