A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7730n54



Internal ID22775625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10631001..10804226hg38UCSC Ensembl
chr21:10708231..10881456hg19UCSC Ensembl
chr21:9730102..9903327hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38173226
hg19173226
hg18173226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586892, nsv586896, nsv586891
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7730n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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