A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063695



Internal ID19152914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42973270..43252073hg38UCSC Ensembl
Innerchr19:43477422..43756225hg19UCSC Ensembl
Innerchr19:48169262..48448065hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38278804
hg19278804
hg18278804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3577n100
Supporting Variantsnssv3570191
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)nsv1063695
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