A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550739



Internal ID15991462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46259024hg38UCSC Ensembl
Innerchr10:47543322..47630260hg19UCSC Ensembl
Innerchr10:47013328..47100266hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3886939
hg1986939
hg1886939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1107n54
Supporting Variantsnssv1173573
SamplesHGDP00907
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550739
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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