A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999584



Internal ID19159121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29381696..29780258hg38UCSC Ensembl
Innerchr4:29383318..29781880hg19UCSC Ensembl
Innerchr4:28992416..29390978hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38398563
hg19398563
hg18398563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620634
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)nsv999584
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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