A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518390



Internal ID15445683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5846277..5853561hg38UCSC Ensembl
Innerchr1:5906337..5913621hg19UCSC Ensembl
Innerchr1:5828924..5836208hg18UCSC Ensembl
Innerchr1:5840603..5847887hg17UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg387285
hg197285
hg187285
hg177285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695820
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518390
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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