A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058364



Internal ID19147583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43052691..43109111hg38UCSC Ensembl
Innerchr19:43556843..43613263hg19UCSC Ensembl
Innerchr19:48248683..48305103hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3856421
hg1956421
hg1856421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3586n100
Supporting Variantsnssv3571792, nssv3571793
Samples
Known GenesPSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058364
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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