A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050316



Internal ID18792847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46527218..46591179hg38UCSC Ensembl
Innerchr10:46958438..47022399hg19UCSC Ensembl
Innerchr10:46378444..46442405hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3863962
hg1963962
hg1863962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv760n100
Supporting Variantsnssv3520746
Samples
Known GenesGPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050316
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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