A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587832



Internal ID16375241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45028088..45031790hg38UCSC Ensembl
Innerchr21:46448003..46451705hg19UCSC Ensembl
Innerchr21:45272431..45276133hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383703
hg193703
hg183703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948499, nssv948502, nssv948504, nssv948500, nssv948503, nssv948501
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587832
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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