A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv184e55



Internal ID22761134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28630585..28753355hg38UCSC Ensembl
chr4:28632207..28754977hg19UCSC Ensembl
chr4:28241305..28364075hg18UCSC Ensembl
chr4:28308476..28431246hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38122771
hg19122771
hg18122771
hg17122771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34271, esv34764
SamplesNA18959, NA18956
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv184e55
Frequency
Sample Size771
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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