A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549817



Internal ID15990540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3081241..3085787hg38UCSC Ensembl
Innerchr10:3123433..3127979hg19UCSC Ensembl
Innerchr10:3113433..3117979hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg384547
hg194547
hg184547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740242
Samples
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549817
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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