A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1871n100



Internal ID20153487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37087152..37201854hg38UCSC Ensembl
chr14:37556357..37671059hg19UCSC Ensembl
chr14:36626108..36740810hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38114703
hg19114703
hg18114703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050174, nsv1043410
Samples
Known GenesMIPOL1, SLC25A21, SLC25A21-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1871n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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