A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740239



Internal ID15687509
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 StatusS
Merged Variantsnsv549814
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)nssv740239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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