A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5841n100



Internal ID22791928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176126233..176269841hg38UCSC Ensembl
chr5:175553236..175696844hg19UCSC Ensembl
chr5:175485842..175629450hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38143609
hg19143609
hg18143609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031669, nsv1027784, nsv1032255
Samples
Known GenesLOC643201, SIMC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5841n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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