A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552171



Internal ID15992894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110322242..110575998hg38UCSC Ensembl
Innerchr10:112082000..112335756hg19UCSC Ensembl
Innerchr10:112071990..112325746hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38253757
hg19253757
hg18253757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175009
Samples1780862435_A
Known GenesDUSP5, SMC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552171
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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