A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7727n54



Internal ID22775622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10627687..10813996hg38UCSC Ensembl
chr21:10698461..10884770hg19UCSC Ensembl
chr21:9720332..9906641hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38186310
hg19186310
hg18186310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586879, nsv586877, nsv586883, nsv586880, nsv586890, nsv586882, nsv586881, nsv586878, nsv586884
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7727n54
Frequency
Sample Size17421
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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