A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856593



Internal ID16150549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46411801..46465368hg38UCSC Ensembl
Innerchr16:46445713..46499280hg19UCSC Ensembl
Innerchr16:45003214..45056781hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3853568
hg1953568
hg1853568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572495
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv856593
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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