A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587661



Internal ID16375070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43010215..43028608hg38UCSC Ensembl
Innerchr21:44430325..44448718hg19UCSC Ensembl
Innerchr21:43303394..43321787hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3818394
hg1918394
hg1818394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947405
Samples
Known GenesPKNOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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