A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587802



Internal ID16028525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44485022..44508296hg38UCSC Ensembl
Innerchr21:45904905..45928179hg19UCSC Ensembl
Innerchr21:44729333..44752607hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3823275
hg1923275
hg1823275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948398
Samples
Known GenesTSPEAR, TSPEAR-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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