A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039078



Internal ID18781609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46314355hg38UCSC Ensembl
Innerchr10:47541177..47685591hg19UCSC Ensembl
Innerchr10:47011183..47155597hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38144415
hg19144415
hg18144415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3515493, nssv3515904, nssv3510610, nssv3506022, nssv3507223, nssv3514611, nssv3505924, nssv3512352
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039078
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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