A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21002



Internal ID15827157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24445205..24448396hg38UCSC Ensembl
Outerchr15:24442595..24449855hg38UCSC Ensembl
Innerchr15:24690352..24693543hg19UCSC Ensembl
Outerchr15:24687742..24695002hg19UCSC Ensembl
Innerchr15:22241445..22244636hg18UCSC Ensembl
Outerchr15:22238835..22246095hg18UCSC Ensembl
Innerchr15:22241445..22244636hg17UCSC Ensembl
Outerchr15:22238835..22246095hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387261
hg197261
hg187261
hg177261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA07029
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)nssv21002
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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