A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570687



Internal ID18868968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24198004..24413936hg38UCSC Ensembl
Innerchr19:24380806..24596738hg19UCSC Ensembl
Innerchr19:24172646..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38215933
hg19215933
hg18215933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060045
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3570687
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer