A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587140



Internal ID16374549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18407757..18434164hg38UCSC Ensembl
Innerchr21:19780074..19806481hg19UCSC Ensembl
Innerchr21:18701945..18728352hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3826408
hg1926408
hg1826408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150980
SamplesNINDS_186
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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