A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25810



Internal ID15842178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72649792..72669836hg38UCSC Ensembl
Outerchr15:72649032..72670022hg38UCSC Ensembl
Innerchr15:72942133..72962177hg19UCSC Ensembl
Outerchr15:72941373..72962363hg19UCSC Ensembl
Innerchr15:70729187..70749230hg18UCSC Ensembl
Outerchr15:70728427..70749416hg18UCSC Ensembl
Innerchr15:70729187..70749230hg17UCSC Ensembl
Outerchr15:70728427..70749416hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3820991
hg1920991
hg1820990
hg1720990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9275
Supporting Variants
SamplesNA19132
Known GenesGOLGA6B
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)nssv25810
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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