A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5346n100



Internal ID20156962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102232552..102285398hg38UCSC Ensembl
chr4:103153709..103206555hg19UCSC Ensembl
chr4:103372732..103425578hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3852847
hg1952847
hg1852847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008680, nsv1011868, nsv999012
Samples
Known GenesSLC39A8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5346n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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