A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4251n100



Internal ID20155867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14647016..15324612hg38UCSC Ensembl
chr20:14627662..15305258hg19UCSC Ensembl
chr20:14575662..15253258hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38677597
hg19677597
hg18677597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065152, nsv1066070
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4251n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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