A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100880



Internal ID21279850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:29096975..29105774hg38UCSC Ensembl
Innerchr21:30469296..30478095hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116832
Supporting Variants
Samplessample29
Known GenesMAP3K7CL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100880
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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