A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv262e55



Internal ID20126741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112598225..112819173hg38UCSC Ensembl
chr9:115360505..115581453hg19UCSC Ensembl
chr9:114400326..114621274hg18UCSC Ensembl
chr9:112440060..112661008hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38220949
hg19220949
hg18220949
hg17220949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34739, esv35051, esv34346, esv34763
SamplesNA19209, NA19210, NA19211, NA19204
Known GenesINIP, KIAA1958, SNX30
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)dgv262e55
Frequency
Sample Size771
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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