A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046736



Internal ID18789267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46324327hg38UCSC Ensembl
Innerchr10:47541177..47695563hg19UCSC Ensembl
Innerchr10:47011183..47165569hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38154387
hg19154387
hg18154387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3706018, nssv3510402, nssv3511806, nssv3510532, nssv3510672, nssv3505714, nssv3706019, nssv3706017, nssv3507533, nssv3509465, nssv3521527
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)nsv1046736
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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