A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571251



Internal ID16358660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3153034..3201522hg38UCSC Ensembl
Innerchr16:3203035..3251522hg19UCSC Ensembl
Innerchr16:3143036..3191523hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3848489
hg1948488
hg1848488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4874n54
Supporting Variantsnssv1148907
SamplesHGDP01064
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571251
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