A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587567



Internal ID16028290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41865721..41898934hg38UCSC Ensembl
Innerchr21:43285830..43319043hg19UCSC Ensembl
Innerchr21:42158899..42192112hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3833214
hg1933214
hg1833214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7849n54
Supporting Variantsnssv947146
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587567
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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