A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594001



Internal ID16381410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38464035..38522477hg38UCSC Ensembl
Innerchr4:38465656..38524098hg19UCSC Ensembl
Innerchr4:38142051..38200493hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3858443
hg1958443
hg1858443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995918
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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