A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525775



Internal ID15106382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42677630..42679597hg38UCSC Ensembl
Innerchr21:44097740..44099707hg19UCSC Ensembl
Innerchr21:42970809..42972776hg18UCSC Ensembl
Innerchr21:42970809..42972776hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381968
hg191968
hg181968
hg171968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701947
Samples
Known GenesPDE9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525775
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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