A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527856



Internal ID15455149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96232752..96291833hg38UCSC Ensembl
Innerchr3:95951596..96010677hg19UCSC Ensembl
Innerchr3:97434286..97493367hg18UCSC Ensembl
Innerchr3:97434286..97493367hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3859082
hg1959082
hg1859082
hg1759082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704354
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527856
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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