A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528063



Internal ID15455356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:111251280..111301221hg38UCSC Ensembl
Innerchr10:113011038..113060979hg19UCSC Ensembl
Innerchr10:113001028..113050969hg18UCSC Ensembl
Innerchr10:113001028..113050969hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3849942
hg1949942
hg1849942
hg1749942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704599
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528063
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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