A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519099



Internal ID15099706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113718000..113731648hg38UCSC Ensembl
Innerchr3:113436847..113450495hg19UCSC Ensembl
Innerchr3:114919537..114933185hg18UCSC Ensembl
Innerchr3:114919537..114933185hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3813649
hg1913649
hg1813649
hg1713649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696573
Samples
Known GenesNAA50
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519099
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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