A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520326



Internal ID15447619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73439519..73440760hg38UCSC Ensembl
Innerchr3:73488670..73489911hg19UCSC Ensembl
Innerchr3:73571360..73572601hg18UCSC Ensembl
Innerchr3:73571360..73572601hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381242
hg191242
hg181242
hg171242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694375
Samples
Known GenesPDZRN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520326
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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