A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549890



Internal ID16337299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5597944..5615564hg38UCSC Ensembl
Innerchr10:5639907..5657527hg19UCSC Ensembl
Innerchr10:5679913..5697533hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3817621
hg1917621
hg1817621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174112
SamplesHGDP00893
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549890
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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