A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1e55



Internal ID22760951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:817186..864083hg38UCSC Ensembl
chr1:752566..799463hg19UCSC Ensembl
chr1:742429..789326hg18UCSC Ensembl
chr1:792429..839326hg17UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3846898
hg1946898
hg1846898
hg1746898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34886, esv34681
SamplesNA18947, NA18620
Known GenesFAM87B, LINC00115, LINC01128
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv1e55
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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