A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899746



Internal ID16193702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43155365hg38UCSC Ensembl
Innerchr19:43374601..43659517hg19UCSC Ensembl
Innerchr19:48066441..48351357hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38284917
hg19284917
hg18284917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579723
Supporting Variants
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)nssv899746
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