A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1903n100



Internal ID22787990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44712945..44764023hg38UCSC Ensembl
chr14:45182148..45233226hg19UCSC Ensembl
chr14:44251898..44302976hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3851079
hg1951079
hg1851079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041277, nsv1046279, nsv1049204, nsv1040497, nsv1044764, nsv1047319, nsv1052760
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1903n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss128
Observed Complex0
Frequencyn/a


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