A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571618



Internal ID16359027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20467402..20518912hg38UCSC Ensembl
Innerchr16:20478724..20530234hg19UCSC Ensembl
Innerchr16:20386225..20437735hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3851511
hg1951511
hg1851511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4943n54
Supporting Variantsnssv1149621
SamplesHGDP00932
Known GenesACSM2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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