A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579630



Internal ID16020353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42400086..42402231hg38UCSC Ensembl
Innerchr19:42904238..42906383hg19UCSC Ensembl
Innerchr19:47596078..47598223hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382146
hg192146
hg182146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6460n54
Supporting Variantsnssv899602
Samples
Known GenesLIPE, LIPE-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579630
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