A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv187e55



Internal ID22761137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70360836..70386524hg38UCSC Ensembl
chr4:71226553..71252241hg19UCSC Ensembl
chr4:71261142..71286830hg18UCSC Ensembl
chr4:71407313..71433001hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3825689
hg1925689
hg1825689
hg1725689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv35118, esv34365
SamplesNA18564, NA18623
Known GenesSMR3A, SMR3B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv187e55
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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