A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523851



Internal ID15451144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11805242..11840555hg38UCSC Ensembl
Innerchr10:11847241..11882554hg19UCSC Ensembl
Innerchr10:11887247..11922560hg18UCSC Ensembl
Innerchr10:11887247..11922560hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3835314
hg1935314
hg1835314
hg1735314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699686
Samples
Known GenesPROSER2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523851
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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