A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579705



Internal ID16367114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42866627..43131532hg38UCSC Ensembl
Innerchr19:43370779..43635684hg19UCSC Ensembl
Innerchr19:48062619..48327524hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38264906
hg19264906
hg18264906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6474n54
Supporting Variantsnssv899716
Samples
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579705
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