A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551949



Internal ID16339358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94402684..94403263hg38UCSC Ensembl
Innerchr10:96162441..96163020hg19UCSC Ensembl
Innerchr10:96152431..96153010hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38580
hg19580
hg18580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv755883, nssv755882
Samples
Known GenesTBC1D12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551949
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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