A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740238



Internal ID15687508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3035272..3691194hg38UCSC Ensembl
Innerchr10:3077464..3733386hg19UCSC Ensembl
Innerchr10:3067464..3723386hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38655923
hg19655923
hg18655923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549810
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)nssv740238
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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