A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587651



Internal ID16375060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42583335..42600313hg38UCSC Ensembl
Innerchr21:44003445..44020423hg19UCSC Ensembl
Innerchr21:42876514..42893492hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816979
hg1916979
hg1816979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947397
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587651
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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