A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587841



Internal ID16028564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45199925..45227163hg38UCSC Ensembl
Innerchr21:46619840..46647078hg19UCSC Ensembl
Innerchr21:45444268..45471506hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3827239
hg1927239
hg1827239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948530
Samples
Known GenesADARB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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