A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552094



Internal ID16339503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105358078..105535424hg38UCSC Ensembl
Innerchr10:107117836..107295182hg19UCSC Ensembl
Innerchr10:107107826..107285172hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38177347
hg19177347
hg18177347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1377n54
Supporting Variantsnssv756243, nssv756244
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552094
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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