A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049979



Internal ID18792510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46332046hg38UCSC Ensembl
Innerchr10:47541177..47703282hg19UCSC Ensembl
Innerchr10:47011183..47173288hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38162106
hg19162106
hg18162106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3507186, nssv3511401
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)nsv1049979
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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