A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519387



Internal ID15446680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112778993..112796148hg38UCSC Ensembl
Innerchr4:113700149..113717304hg19UCSC Ensembl
Innerchr4:113919598..113936753hg18UCSC Ensembl
Innerchr4:114057753..114074908hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3817156
hg1917156
hg1817156
hg1717156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696826
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519387
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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