A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586892



Internal ID16374301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10631001..10804226hg38UCSC Ensembl
Innerchr21:10708231..10881456hg19UCSC Ensembl
Innerchr21:9730102..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 Variantsdgv7730n54
Supporting Variantsnssv944781
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586892
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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