A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740235



Internal ID15687505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2382612..3165440hg38UCSC Ensembl
Innerchr10:2424806..3207632hg19UCSC Ensembl
Innerchr10:2414806..3197632hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38782829
hg19782827
hg18782827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549801
Supporting Variants
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)nssv740235
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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