A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5082n100



Internal ID19015450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2956087..3017315hg38UCSC Ensembl
chr4:2957814..3019042hg19UCSC Ensembl
chr4:2927612..2988840hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3861229
hg1961229
hg1861229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014675, nsv1008527, nsv1008781
Samples
Known GenesGRK4, NOP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5082n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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