A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550771



Internal ID15991494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46216824..46281263hg38UCSC Ensembl
Innerchr10:47588060..47652499hg19UCSC Ensembl
Innerchr10:47058066..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3864440
hg1964440
hg1864440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1114n54
Supporting Variantsnssv1174505
SamplesHGDP00682
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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