A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571164



Internal ID16358573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1482836..1510110hg38UCSC Ensembl
Innerchr16:1532837..1560111hg19UCSC Ensembl
Innerchr16:1472838..1500112hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3827275
hg1927275
hg1827275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4854n54
Supporting Variantsnssv1148892
SamplesHGDP00546
Known GenesPTX4, TELO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571164
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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