A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv89e55



Internal ID20126568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95292222..95675258hg38UCSC Ensembl
chr14:95758559..96141595hg19UCSC Ensembl
chr14:94828312..95211348hg18UCSC Ensembl
chr14:94828312..95211348hg17UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38383037
hg19383037
hg18383037
hg17383037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2751290, esv2751289
SamplesBEC_701, BEC_632
Known GenesCLMN, GLRX5, LINC00341, SCARNA13, SNHG10, SYNE3, TCL6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv89e55
Frequency
Sample Size771
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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