A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039231



Internal ID18781762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3131146..3736633hg38UCSC Ensembl
Innerchr10:3173338..3778825hg19UCSC Ensembl
Innerchr10:3163338..3768825hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38605488
hg19605488
hg18605488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3500935, nssv3493527
Samples
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039231
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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