A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21736



Internal ID15835572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28635242..28635718hg38UCSC Ensembl
Outerchr15:28634797..28636624hg38UCSC Ensembl
Innerchr15:28880388..28880864hg19UCSC Ensembl
Outerchr15:28879943..28881770hg19UCSC Ensembl
Innerchr15:26679429..26679905hg18UCSC Ensembl
Outerchr15:26678984..26680811hg18UCSC Ensembl
Innerchr15:26679429..26679905hg17UCSC Ensembl
Outerchr15:26678984..26680811hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381828
hg191828
hg181828
hg171828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9216
Supporting Variants
SamplesNA18552
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)nssv21736
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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