A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522540



Internal ID15449833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4300855..4306204hg38UCSC Ensembl
Innerchr10:4343047..4348396hg19UCSC Ensembl
Innerchr10:4333047..4338396hg18UCSC Ensembl
Innerchr10:4333047..4338396hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385350
hg195350
hg185350
hg175350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705919
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522540
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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