A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587076



Internal ID16027799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15584547..15772692hg38UCSC Ensembl
Innerchr21:16956866..17145011hg19UCSC Ensembl
Innerchr21:15878737..16066882hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38188146
hg19188146
hg18188146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151408
Samples1780854261_A
Known GenesUSP25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587076
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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