A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571667



Internal ID18869948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43001832..43225780hg38UCSC Ensembl
Innerchr19:43505984..43729932hg19UCSC Ensembl
Innerchr19:48197824..48421772hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38223949
hg19223949
hg18223949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055880
Supporting Variants
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3571667
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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