A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066044



Internal ID19155263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42845685..42943854hg38UCSC Ensembl
Innerchr19:43349837..43448006hg19UCSC Ensembl
Innerchr19:48041677..48139846hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3898170
hg1998170
hg1898170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723025
Samples
Known GenesPSG1, PSG10P, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066044
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