A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571821



Internal ID16012544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31205588..31213828hg38UCSC Ensembl
Innerchr16:31216909..31225149hg19UCSC Ensembl
Innerchr16:31124410..31132650hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg388241
hg198241
hg188241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4990n54
Supporting Variantsnssv855492, nssv855493, nssv855494, nssv855495, nssv855496
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571821
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer