A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102075



Internal ID21278987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41309157..41318138hg38UCSC Ensembl
Innerchr21:42681084..42690065hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg388982
hg198982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111911
Supporting Variants
Samplessample276
Known GenesFAM3B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102075
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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