A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7833n54



Internal ID22775728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38744120..38785200hg38UCSC Ensembl
chr21:40116044..40157124hg19UCSC Ensembl
chr21:39037914..39078994hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3841081
hg1941081
hg1841081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587475, nsv587476
SamplesHGDP00445, HGDP00232, HGDP00582, HGDP00197, HGDP00206
Known GenesLINC00114
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7833n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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