A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552093



Internal ID16339502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105354916..105539717hg38UCSC Ensembl
Innerchr10:107114674..107299475hg19UCSC Ensembl
Innerchr10:107104664..107289465hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38184802
hg19184802
hg18184802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1377n54
Supporting Variantsnssv756242
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552093
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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