A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587543



Internal ID16374952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41613178..41618764hg38UCSC Ensembl
Innerchr21:43033338..43038924hg19UCSC Ensembl
Innerchr21:41906407..41911993hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385587
hg195587
hg185587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7844n54
Supporting Variantsnssv947043
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587543
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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