A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4239n100



Internal ID22790326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1590079..1601549hg38UCSC Ensembl
chr20:1570725..1582195hg19UCSC Ensembl
chr20:1518725..1530195hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811471
hg1911471
hg1811471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067488, nsv1063159
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4239n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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