A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521941



Internal ID15449234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153809312..153832788hg38UCSC Ensembl
Innerchr3:153527101..153550577hg19UCSC Ensembl
Innerchr3:155009791..155033267hg18UCSC Ensembl
Innerchr3:155009799..155033275hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3823477
hg1923477
hg1823477
hg1723477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694709
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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