A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1918n100



Internal ID22788005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48311535..48450204hg38UCSC Ensembl
chr14:48780738..48919407hg19UCSC Ensembl
chr14:47850488..47989157hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38138670
hg19138670
hg18138670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050803, nsv1041212, nsv1046630, nsv1043059, nsv1048456, nsv1039115, nsv1049661, nsv1041783, nsv1054435
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)dgv1918n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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