A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587386



Internal ID16028109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33321963..33323970hg38UCSC Ensembl
Innerchr21:34694268..34696275hg19UCSC Ensembl
Innerchr21:33616138..33618145hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382008
hg192008
hg182008
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7816n54
Supporting Variantsnssv946633, nssv946634
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587386
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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