A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045329



Internal ID18787860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46261528hg38UCSC Ensembl
Innerchr10:47541177..47632764hg19UCSC Ensembl
Innerchr10:47011183..47102770hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3891588
hg1991588
hg1891588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830n100
Supporting Variantsnssv3508138
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)nsv1045329
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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