A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549889



Internal ID16337298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5568386..5588168hg38UCSC Ensembl
Innerchr10:5610349..5630131hg19UCSC Ensembl
Innerchr10:5600349..5620131hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3819783
hg1919783
hg1819783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743476
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549889
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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