A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594686



Internal ID16382095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:75214681..75287785hg38UCSC Ensembl
Innerchr4:76139891..76212995hg19UCSC Ensembl
Innerchr4:76358915..76432019hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3873105
hg1973105
hg1873105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1002363
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594686
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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