A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587043



Internal ID16027766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14129201..14178114hg38UCSC Ensembl
Innerchr21:15501522..15550435hg19UCSC Ensembl
Innerchr21:14423393..14472306hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3848914
hg1948914
hg1848914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944948
Samples
Known GenesLIPI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587043
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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