A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549814



Internal ID15990537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3055020..3170233hg38UCSC Ensembl
Innerchr10:3097212..3212425hg19UCSC Ensembl
Innerchr10:3087212..3202425hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38115214
hg19115214
hg18115214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740239
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)nsv549814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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