A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5079n100



Internal ID20156695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:843485..970603hg38UCSC Ensembl
chr4:837273..964391hg19UCSC Ensembl
chr4:827273..954391hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38127119
hg19127119
hg18127119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010196, nsv998496
Samples
Known GenesDGKQ, GAK, TMEM175
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5079n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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