A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579638



Internal ID16367047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42764341..42851743hg38UCSC Ensembl
Innerchr19:43268493..43355895hg19UCSC Ensembl
Innerchr19:47960333..48047735hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3887403
hg1987403
hg1887403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6461n54
Supporting Variantsnssv899610
Samples
Known GenesLOC100289650, PSG10P, PSG8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579638
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