A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552248



Internal ID16339657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122146687..122161269hg38UCSC Ensembl
Innerchr10:123906202..123920784hg19UCSC Ensembl
Innerchr10:123896192..123910774hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3814583
hg1914583
hg1814583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760314
Samples
Known GenesTACC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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