A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571543



Internal ID16012266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886390..15911711hg38UCSC Ensembl
Innerchr16:15980247..16005568hg19UCSC Ensembl
Innerchr16:15887748..15913069hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3825322
hg1925322
hg1825322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150548
SamplesHGDP01202
Known GenesFOPNL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571543
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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