A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv947401



Internal ID15894671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42665548..42680969hg38UCSC Ensembl
Innerchr21:44085658..44101079hg19UCSC Ensembl
Innerchr21:42958727..42974148hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3815422
hg1915422
hg1815422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587655
Supporting Variants
Samples
Known GenesPDE9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv947401
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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