A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054118



Internal ID18796649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46262585hg38UCSC Ensembl
Innerchr10:47541177..47633821hg19UCSC Ensembl
Innerchr10:47011183..47103827hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3892645
hg1992645
hg1892645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830n100
Supporting Variantsnssv3520323, nssv3516298
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054118
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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