A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099954



Internal ID21275589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62936967..62941590hg38UCSC Ensembl
Innerchr20:61568319..61572942hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384624
hg194624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112004
Supporting Variants
Samplessample224
Known GenesDIDO1, GID8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099954
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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