A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516059



Internal ID15443352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114318373..114366175hg38UCSC Ensembl
Innerchr4:115239529..115287331hg19UCSC Ensembl
Innerchr4:115458978..115506780hg18UCSC Ensembl
Innerchr4:115597133..115644935hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3847803
hg1947803
hg1847803
hg1747803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659384, nssv665934
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516059
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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