A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521479



Internal ID15448772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38456381..38462820hg38UCSC Ensembl
Innerchr1:38922053..38928492hg19UCSC Ensembl
Innerchr1:38694640..38701079hg18UCSC Ensembl
Innerchr1:38591146..38597585hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386440
hg196440
hg186440
hg176440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694450
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521479
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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