A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852819



Internal ID15800089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15856272..15856938hg38UCSC Ensembl
Innerchr16:15950129..15950795hg19UCSC Ensembl
Innerchr16:15857630..15858296hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38667
hg19667
hg18667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571540
Supporting Variants
Samples
Known GenesMYH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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