A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv263e55



Internal ID22761213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135225315..135442209hg38UCSC Ensembl
chr9:138117161..138334055hg19UCSC Ensembl
chr9:137256982..137473876hg18UCSC Ensembl
chr9:135343106..135560000hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38216895
hg19216895
hg18216895
hg17216895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752283, esv2752284, esv2752282
SamplesBEC_131, BEC_22, BEC_311
Known GenesC9orf62
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)dgv263e55
Frequency
Sample Size771
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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