A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594368



Internal ID16381777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62819236..62879098hg38UCSC Ensembl
Innerchr4:63684954..63744816hg19UCSC Ensembl
Innerchr4:63367549..63427411hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3859863
hg1959863
hg1859863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1000549
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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