A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549812



Internal ID15990535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3044294..3125271hg38UCSC Ensembl
Innerchr10:3086486..3167463hg19UCSC Ensembl
Innerchr10:3076486..3157463hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3880978
hg1980978
hg1880978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv935n54
Supporting Variantsnssv1174105
SamplesHGDP00465
Known GenesPFKP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549812
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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