A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587625



Internal ID16375034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42111443..42137588hg38UCSC Ensembl
Innerchr21:43531553..43557698hg19UCSC Ensembl
Innerchr21:42404622..42430767hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3826146
hg1926146
hg1826146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947349
Samples
Known GenesUMODL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587625
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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