A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550791



Internal ID15991514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46238316..46332377hg38UCSC Ensembl
Innerchr10:47609552..47703613hg19UCSC Ensembl
Innerchr10:47079558..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3894062
hg1994062
hg1894062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1115n54
Supporting Variantsnssv1174534
SamplesHGDP01019
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550791
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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