A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21835



Internal ID15840746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20333969..20441106hg38UCSC Ensembl
Outerchr15:20331306..20441694hg38UCSC Ensembl
Innerchr15:20539222..20646359hg19UCSC Ensembl
Outerchr15:20536559..20646947hg19UCSC Ensembl
Innerchr15:18799236..18906373hg18UCSC Ensembl
Outerchr15:18796573..18906961hg18UCSC Ensembl
Innerchr15:18799236..18906373hg17UCSC Ensembl
Outerchr15:18796573..18906961hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38110389
hg19110389
hg18110389
hg17110389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18980
Known GenesHERC2P3
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)nssv21835
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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