A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1985n100



Internal ID20153601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105563288..106321074hg38UCSC Ensembl
chr14:106029625..106777331hg19UCSC Ensembl
chr14:105100670..105848376hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38757787
hg19747707
hg18747707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036027, nsv1038977
Samples
Known GenesADAM6, ELK2AP, KIAA0125, LINC00226, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1985n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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