A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519201



Internal ID15446494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4353051..4356988hg38UCSC Ensembl
Innerchr4:4354778..4358715hg19UCSC Ensembl
Innerchr4:4405679..4409616hg18UCSC Ensembl
Innerchr4:4472850..4476787hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg383938
hg193938
hg183938
hg173938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696685
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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