A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594118



Internal ID16034841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:47558369..47915713hg38UCSC Ensembl
Innerchr4:47560386..47917730hg19UCSC Ensembl
Innerchr4:47255143..47612487hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38357345
hg19357345
hg18357345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv997558
Samples
Known GenesATP10D, CORIN, MIR8053, NFXL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594118
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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