A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2161n100



Internal ID22788248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106688061..106877229hg38UCSC Ensembl
chr14:107144078..107285437hg19UCSC Ensembl
chr14:106215123..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38189169
hg19141360
hg18141360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035139, nsv1049472, nsv1048445, nsv1040793, nsv1049475
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)dgv2161n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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