A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594476



Internal ID16381885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64872115..65284951hg38UCSC Ensembl
Innerchr4:65737833..66150669hg19UCSC Ensembl
Innerchr4:65420428..65833264hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38412837
hg19412837
hg18412837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1001741
Samples
Known GenesLOC401134
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594476
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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