A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571544



Internal ID16012267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886390..15924732hg38UCSC Ensembl
Innerchr16:15980247..16018589hg19UCSC Ensembl
Innerchr16:15887748..15926090hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3838343
hg1938343
hg1838343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4926n54
Supporting Variantsnssv1150549, nssv1150551, nssv852821, nssv1150550, nssv1150552
SamplesHGDP01201, HGDP00906, HGDP00907, HGDP00928
Known GenesFOPNL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571544
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