A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551759



Internal ID16339168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84840324..85032590hg38UCSC Ensembl
Innerchr10:86600080..86792346hg19UCSC Ensembl
Innerchr10:86590060..86782326hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38192267
hg19192267
hg18192267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752188
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551759
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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