A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7764n54



Internal ID22775659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14514598..14534269hg38UCSC Ensembl
chr21:15886919..15906590hg19UCSC Ensembl
chr21:14808790..14828461hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3819672
hg1919672
hg1819672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587046, nsv587045
Samples
Known GenesSAMSN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7764n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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