A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150543



Internal ID15525956
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571527
Supporting Variants
SamplesHGDP00005
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150543
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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