A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152414



Internal ID15527624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42752792..42768002hg38UCSC Ensembl
Innerchr21:44172902..44188112hg19UCSC Ensembl
Innerchr21:43045971..43061181hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3815211
hg1915211
hg1815211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587658
Supporting Variants
SamplesHGDP00521
Known GenesPDE9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152414
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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