A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594104



Internal ID16381513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:45103193..45663811hg38UCSC Ensembl
Innerchr4:45105210..45665828hg19UCSC Ensembl
Innerchr4:44799967..45360585hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38560619
hg19560619
hg18560619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv996903
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594104
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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