A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593645



Internal ID16381054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8692663..8727745hg38UCSC Ensembl
Innerchr4:8694389..8729471hg19UCSC Ensembl
Innerchr4:8745289..8780371hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3835083
hg1935083
hg1835083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv991254
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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