A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039508



Internal ID18782039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48387675..48446360hg38UCSC Ensembl
Innerchr10:49595718..49654403hg19UCSC Ensembl
Innerchr10:49265724..49324409hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3858686
hg1958686
hg1858686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505998
Samples
Known GenesARHGAP22, MAPK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039508
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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