A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1870n100



Internal ID22787957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37029636..37077154hg38UCSC Ensembl
chr14:37498841..37546359hg19UCSC Ensembl
chr14:36568592..36616110hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3847519
hg1947519
hg1847519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037719, nsv1048854, nsv1036201
Samples
Known GenesSLC25A21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1870n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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