A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549819



Internal ID15990542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3082324..3085303hg38UCSC Ensembl
Innerchr10:3124516..3127495hg19UCSC Ensembl
Innerchr10:3114516..3117495hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg382980
hg192980
hg182980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740244
Samples
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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