A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23562



Internal ID15496160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34535791..34552889hg38UCSC Ensembl
Outerchr15:34535249..34554085hg38UCSC Ensembl
Innerchr15:34827992..34845090hg19UCSC Ensembl
Outerchr15:34827450..34846286hg19UCSC Ensembl
Innerchr15:32615284..32632382hg18UCSC Ensembl
Outerchr15:32614742..32633578hg18UCSC Ensembl
Innerchr15:32615284..32632382hg17UCSC Ensembl
Outerchr15:32614742..32633578hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3818837
hg1918837
hg1818837
hg1718837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA19144
Known GenesGOLGA8B
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)nssv23562
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