A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852529



Internal ID15799799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11218316..11302493hg38UCSC Ensembl
Innerchr16:11312173..11396350hg19UCSC Ensembl
Innerchr16:11219674..11303851hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3884178
hg1984178
hg1884178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571453
Supporting Variants
Samples
Known GenesPRM1, PRM2, PRM3, SOCS1, TNP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852529
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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