A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550797



Internal ID16338206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46287904..46332377hg38UCSC Ensembl
Innerchr10:47659140..47703613hg19UCSC Ensembl
Innerchr10:47129146..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3844474
hg1944474
hg1844474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1118n54
Supporting Variantsnssv1174538, nssv747637, nssv1174540, nssv1174539
SamplesHGDP01384, HGDP00919, HGDP00743
Known GenesANTXRL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550797
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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