A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1982n100



Internal ID20153598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105521689..106043007hg38UCSC Ensembl
chr14:105988026..106499238hg19UCSC Ensembl
chr14:105059071..105570283hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38521319
hg19511213
hg18511213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045210, nsv1036562, nsv1050073
Samples
Known GenesADAM6, ELK2AP, KIAA0125, MIR8071-1, MIR8071-2, TMEM121
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1982n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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