A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv206e55



Internal ID22761156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:129322738..129427181hg38UCSC Ensembl
chr5:128658431..128762874hg19UCSC Ensembl
chr5:128686330..128790773hg18UCSC Ensembl
chr5:128686330..128790773hg17UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38104444
hg19104444
hg18104444
hg17104444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv35072, esv34881
SamplesNA07029, NA07000
Known GenesMIR4460
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)dgv206e55
Frequency
Sample Size771
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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