A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525722



Internal ID15453015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:741956..754428hg38UCSC Ensembl
Innerchr10:787896..800368hg19UCSC Ensembl
Innerchr10:777896..790368hg18UCSC Ensembl
Innerchr10:777896..790368hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3812473
hg1912473
hg1812473
hg1712473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n21
Supporting Variantsnssv701886
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525722
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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