A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579633



Internal ID16020356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42421484..42425102hg38UCSC Ensembl
Innerchr19:42925636..42929254hg19UCSC Ensembl
Innerchr19:47617476..47621094hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383619
hg193619
hg183619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899605
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)nsv579633
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