A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045654



Internal ID19134873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114894815..115119719hg38UCSC Ensembl
Innerchr10:116654574..116879483hg19UCSC Ensembl
Innerchr10:116644564..116869473hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38224905
hg19224910
hg18224910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv977n100
Supporting Variantsnssv3706242
Samples
Known GenesATRNL1, FAM160B1, TRUB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045654
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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