A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579772



Internal ID16367181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43001832..43191688hg38UCSC Ensembl
Innerchr19:43505984..43695840hg19UCSC Ensembl
Innerchr19:48197824..48387680hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38189857
hg19189857
hg18189857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6488n54
Supporting Variantsnssv1149965, nssv1149963, nssv1149964, nssv1149966
Samples1782681164_A, HGDP00696, HGDP01274, 1780854499_A
Known GenesPSG11, PSG2, PSG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579772
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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