A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594985



Internal ID16382394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103607152..103656225hg38UCSC Ensembl
Innerchr4:104528309..104577382hg19UCSC Ensembl
Innerchr4:104747758..104796831hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3849074
hg1949074
hg1849074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1003648
Samples
Known GenesTACR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594985
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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