A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4397n100



Internal ID22790484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:20202324..20276862hg38UCSC Ensembl
chr21:21574637..21649174hg19UCSC Ensembl
chr21:20496508..20571045hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3874539
hg1974538
hg1874538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060546, nsv1059156
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4397n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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