A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587014



Internal ID16374423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13585652..13843493hg38UCSC Ensembl
Innerchr21:14957973..15215814hg19UCSC Ensembl
Innerchr21:13879844..14137685hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38257842
hg19257842
hg18257842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944916
Samples
Known GenesC21orf15, LOC100288966, MIR8069, POTED
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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