A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5501n100



Internal ID22791588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:188015795..188951696hg38UCSC Ensembl
chr4:188936949..189872850hg19UCSC Ensembl
chr4:189173943..190109844hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38935902
hg19935902
hg18935902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017310, nsv1020663
Samples
Known GenesLINC01060, TRIML1, TRIML2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5501n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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