A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24432



Internal ID15844475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28657561..28664300hg38UCSC Ensembl
Outerchr15:28657413..28665794hg38UCSC Ensembl
Innerchr15:28902707..28909446hg19UCSC Ensembl
Outerchr15:28902559..28910940hg19UCSC Ensembl
Innerchr15:26701748..26708487hg18UCSC Ensembl
Outerchr15:26701600..26709981hg18UCSC Ensembl
Innerchr15:26701748..26708487hg17UCSC Ensembl
Outerchr15:26701600..26709981hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg388382
hg198382
hg188382
hg178382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9217
Supporting Variants
SamplesNA19240
Known GenesHERC2P9
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)nssv24432
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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