A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571294



Internal ID16358703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315518..4316990hg38UCSC Ensembl
Innerchr16:4365519..4366991hg19UCSC Ensembl
Innerchr16:4305520..4306992hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381473
hg191473
hg181473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4883n54
Supporting Variantsnssv852330
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571294
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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