A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5069n100



Internal ID20156685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59167..121670hg38UCSC Ensembl
chr4:59060..121550hg19UCSC Ensembl
chr4:49060..111550hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3862504
hg1962491
hg1862491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999801, nsv1006722, nsv1004352, nsv1007526, nsv998652, nsv1012461, nsv1000949, nsv1004722, nsv1014389, nsv1013362, nsv999168
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5069n100
Frequency
Sample Size29084
Observed Gain65
Observed Loss0
Observed Complex0
Frequencyn/a


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