A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25544



Internal ID15833128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24405686..24426572hg38UCSC Ensembl
Outerchr15:24405369..24426951hg38UCSC Ensembl
Innerchr15:24650833..24671719hg19UCSC Ensembl
Outerchr15:24650516..24672098hg19UCSC Ensembl
Innerchr15:22201926..22222812hg18UCSC Ensembl
Outerchr15:22201609..22223191hg18UCSC Ensembl
Innerchr15:22201926..22222812hg17UCSC Ensembl
Outerchr15:22201609..22223191hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3821583
hg1921583
hg1821583
hg1721583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18502
Known Genes
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)nssv25544
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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