A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008424



Internal ID19097642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13278..47091hg38UCSC Ensembl
Innerchr4:13278..47087hg19UCSC Ensembl
Innerchr4:3278..37087hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3833814
hg1933810
hg1833810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5052n100
Supporting Variantsnssv3615223
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008424
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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