A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549802



Internal ID15990525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2461200..3253481hg38UCSC Ensembl
Innerchr10:2503394..3295673hg19UCSC Ensembl
Innerchr10:2493394..3285673hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38792282
hg19792280
hg18792280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv932n54
Supporting Variantsnssv740236
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)nsv549802
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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