A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552620



Internal ID16340029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133291903..133292176hg38UCSC Ensembl
Innerchr10:135105407..135105680hg19UCSC Ensembl
Innerchr10:134955397..134955670hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38274
hg19274
hg18274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1481n54
Supporting Variantsnssv762563
Samples
Known GenesTUBGCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552620
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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