A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25635



Internal ID15484387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43215019..43253602hg38UCSC Ensembl
Outerchr19:43212049..43254069hg38UCSC Ensembl
Innerchr19:43719171..43757754hg19UCSC Ensembl
Outerchr19:43716201..43758221hg19UCSC Ensembl
Innerchr19:48411011..48449594hg18UCSC Ensembl
Outerchr19:48408041..48450061hg18UCSC Ensembl
Innerchr19:48411011..48449594hg17UCSC Ensembl
Outerchr19:48408041..48450061hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3842021
hg1942021
hg1842021
hg1742021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9730
Supporting Variants
SamplesNA12740
Known GenesLOC284344, PSG9
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv25635
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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