A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578235



Internal ID16018958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137402..1138048hg38UCSC Ensembl
Innerchr19:1137401..1138047hg19UCSC Ensembl
Innerchr19:1088401..1089047hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38647
hg19647
hg18647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6191n54
Supporting Variantsnssv891692
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578235
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