A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891828



Internal ID15839098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566560..1572370hg38UCSC Ensembl
Innerchr19:1566559..1572369hg19UCSC Ensembl
Innerchr19:1517559..1523369hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385811
hg195811
hg185811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578306
Supporting Variants
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891828
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