A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552170



Internal ID16339579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109442582..109586455hg38UCSC Ensembl
Innerchr10:111202340..111346213hg19UCSC Ensembl
Innerchr10:111192330..111336203hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38143874
hg19143874
hg18143874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1394n54
Supporting Variantsnssv758424
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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