A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551838



Internal ID16339247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88298880..88377288hg38UCSC Ensembl
Innerchr10:90058637..90137045hg19UCSC Ensembl
Innerchr10:90048617..90127025hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3878409
hg1978409
hg1878409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753221
Samples
Known GenesRNLS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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