A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571430



Internal ID16012153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8974445..9095667hg38UCSC Ensembl
Innerchr16:9068302..9189524hg19UCSC Ensembl
Innerchr16:8975803..9097025hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38121223
hg19121223
hg18121223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150524
SamplesHGDP00776
Known GenesC16orf72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571430
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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