A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593779



Internal ID16381188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16334390..16373541hg38UCSC Ensembl
Innerchr4:16336013..16375164hg19UCSC Ensembl
Innerchr4:15945111..15984262hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3839152
hg1939152
hg1839152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993113
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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