A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4422n100



Internal ID22790509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:27820466..27987620hg38UCSC Ensembl
chr21:29192785..29359939hg19UCSC Ensembl
chr21:28114656..28281810hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38167155
hg19167155
hg18167155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060376, nsv1062092
Samples
Known GenesMIR5009
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4422n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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