A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22276



Internal ID15835620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85214169..85235936hg38UCSC Ensembl
Outerchr15:85208468..85236421hg38UCSC Ensembl
Innerchr15:85757400..85779167hg19UCSC Ensembl
Outerchr15:85751699..85779652hg19UCSC Ensembl
Innerchr15:83558404..83580171hg18UCSC Ensembl
Outerchr15:83552703..83580656hg18UCSC Ensembl
Innerchr15:83558404..83580171hg17UCSC Ensembl
Outerchr15:83552703..83580656hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3827954
hg1927954
hg1827954
hg1727954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9292
Supporting Variants
SamplesNA18552
Known GenesLOC440300
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)nssv22276
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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