A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25074



Internal ID15839646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28635242..28636624hg38UCSC Ensembl
Outerchr15:28634797..28637023hg38UCSC Ensembl
Innerchr15:28880388..28881770hg19UCSC Ensembl
Outerchr15:28879943..28882169hg19UCSC Ensembl
Innerchr15:26679429..26680811hg18UCSC Ensembl
Outerchr15:26678984..26681210hg18UCSC Ensembl
Innerchr15:26679429..26680811hg17UCSC Ensembl
Outerchr15:26678984..26681210hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382227
hg192227
hg182227
hg172227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9216
Supporting Variants
SamplesNA18972
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)nssv25074
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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