A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551188



Internal ID16338597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63586540..63633853hg38UCSC Ensembl
Innerchr10:65346300..65393613hg19UCSC Ensembl
Innerchr10:65016306..65063619hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3847314
hg1947314
hg1847314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748935
Samples
Known GenesREEP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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