A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5783n100



Internal ID22791870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113580701..113620891hg38UCSC Ensembl
chr5:112916398..112956588hg19UCSC Ensembl
chr5:112944297..112984487hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3840191
hg1940191
hg1840191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031336, nsv1029507
Samples
Known GenesYTHDC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5783n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer