A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549818



Internal ID15990541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3081241..3227125hg38UCSC Ensembl
Innerchr10:3123433..3269317hg19UCSC Ensembl
Innerchr10:3113433..3259317hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38145885
hg19145885
hg18145885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740243
Samples
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549818
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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