A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587481



Internal ID16374890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39226795..39255094hg38UCSC Ensembl
Innerchr21:40598721..40627020hg19UCSC Ensembl
Innerchr21:39520591..39548890hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3828300
hg1928300
hg1828300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946777
Samples
Known GenesBRWD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587481
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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