A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4439n100



Internal ID22790526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45894976..45923450hg38UCSC Ensembl
chr21:47314890..47343364hg19UCSC Ensembl
chr21:46139318..46167792hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3828475
hg1928475
hg1828475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062386, nsv1061940
Samples
Known GenesPCBP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4439n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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