A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550734



Internal ID15991457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46166132..46332377hg38UCSC Ensembl
Innerchr10:47537368..47703613hg19UCSC Ensembl
Innerchr10:47007374..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38166246
hg19166246
hg18166246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1109n54
Supporting Variantsnssv747380, nssv747381, nssv747382, nssv747385, nssv747384, nssv747383
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550734
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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