A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519145



Internal ID15099752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8772241..8821239hg38UCSC Ensembl
Innerchr3:8813927..8862925hg19UCSC Ensembl
Innerchr3:8788927..8837925hg18UCSC Ensembl
Innerchr3:8788927..8837925hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3848999
hg1948999
hg1848999
hg1748999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n21
Supporting Variantsnssv694310
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519145
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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