A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587325



Internal ID16374734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:25103871..25260408hg38UCSC Ensembl
Innerchr21:26476184..26632722hg19UCSC Ensembl
Innerchr21:25398055..25554593hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38156538
hg19156539
hg18156539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946581
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587325
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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