A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4329n100



Internal ID20155945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54031269..54053839hg38UCSC Ensembl
chr20:52647808..52670378hg19UCSC Ensembl
chr20:52081215..52103785hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3822571
hg1922571
hg1822571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065888, nsv1065004, nsv1055891, nsv1067336
Samples
Known GenesBCAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4329n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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