A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851754



Internal ID16145710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:766072..768092hg38UCSC Ensembl
Innerchr16:816072..818092hg19UCSC Ensembl
Innerchr16:756073..758093hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382021
hg192021
hg182021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571030
Supporting Variants
Samples
Known GenesMSLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851754
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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