A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26120



Internal ID15491955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34557037..34561072hg38UCSC Ensembl
Outerchr15:34555367..34562688hg38UCSC Ensembl
Innerchr15:34849238..34853273hg19UCSC Ensembl
Outerchr15:34847568..34854889hg19UCSC Ensembl
Innerchr15:32636530..32640565hg18UCSC Ensembl
Outerchr15:32634860..32642181hg18UCSC Ensembl
Innerchr15:32636530..32640565hg17UCSC Ensembl
Outerchr15:32634860..32642181hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg387322
hg197322
hg187322
hg177322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA18860
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)nssv26120
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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