A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7751n54



Internal ID20141175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:12965965..13967777hg38UCSC Ensembl
chr21:14338286..15340098hg19UCSC Ensembl
chr21:13260157..14261969hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg381001813
hg191001813
hg181001813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586985, nsv586988
Samples
Known GenesANKRD20A11P, ANKRD30BP2, C21orf15, LOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7751n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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