A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23534



Internal ID15496161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34428418..34512298hg38UCSC Ensembl
Outerchr15:34427415..34512767hg38UCSC Ensembl
Innerchr15:34720619..34804499hg19UCSC Ensembl
Outerchr15:34719616..34804968hg19UCSC Ensembl
Innerchr15:32507911..32591791hg18UCSC Ensembl
Outerchr15:32506908..32592260hg18UCSC Ensembl
Innerchr15:32507911..32591791hg17UCSC Ensembl
Outerchr15:32506908..32592260hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3885353
hg1985353
hg1885353
hg1785353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA19144
Known GenesGOLGA8A
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)nssv23534
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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