A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101974



Internal ID21271577
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 StatusS
Merged Variantsnsv3110152
Supporting Variants
Samplessample165
Known GenesDSCAM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101974
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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