A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551385



Internal ID16338794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66575771..66837372hg38UCSC Ensembl
Innerchr10:68335529..68597130hg19UCSC Ensembl
Innerchr10:68005535..68267136hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38261602
hg19261602
hg18261602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1234n54
Supporting Variantsnssv1174226
SamplesHGDP01380
Known GenesCTNNA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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