A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27773



Internal ID15491449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36350691..36355949hg38UCSC Ensembl
Outerchr19:36349348..36360275hg38UCSC Ensembl
Innerchr19:36841593..36846851hg19UCSC Ensembl
Outerchr19:36840250..36851177hg19UCSC Ensembl
Innerchr19:41533433..41538691hg18UCSC Ensembl
Outerchr19:41532090..41543017hg18UCSC Ensembl
Innerchr19:41533433..41538691hg17UCSC Ensembl
Outerchr19:41532090..41543017hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3810928
hg1910928
hg1810928
hg1710928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9716
Supporting Variants
SamplesNA18860
Known GenesZFP14
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)nssv27773
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