A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594371



Internal ID16381780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62913570..62968251hg38UCSC Ensembl
Innerchr4:63779288..63833969hg19UCSC Ensembl
Innerchr4:63461883..63516564hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3854682
hg1954682
hg1854682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1000552
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594371
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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