A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578727



Internal ID16019450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669937..15724712hg38UCSC Ensembl
Innerchr19:15780747..15835522hg19UCSC Ensembl
Innerchr19:15641747..15696522hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3854776
hg1954776
hg1854776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6289n54
Supporting Variantsnssv1149845, nssv1149844
SamplesHGDP01413, HGDP00467
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578727
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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