A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852803



Internal ID15800073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15031584..15074903hg38UCSC Ensembl
Innerchr16:15125441..15168760hg19UCSC Ensembl
Innerchr16:15032942..15076261hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3843320
hg1943320
hg1843320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571527
Supporting Variants
Samples
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852803
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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