A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9216



Internal ID15847128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28583805..28656480hg38UCSC Ensembl
Outerchr15:28828951..28901626hg19UCSC Ensembl
Outerchr15:26627992..26700667hg18UCSC Ensembl
Outerchr15:26627992..26700667hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3872676
hg1972676
hg1872676
hg1772676
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25074, nssv25049, nssv22345, nssv25099, nssv27217, nssv25733, nssv23092, nssv21504, nssv24406, nssv21796, nssv25487, nssv21736, nssv22375, nssv21534
SamplesNA18502, NA11830, NA18980, NA18975, NA19221, NA19132, NA19240, NA18972, NA18552
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)nsv9216
Frequency
Sample Size31
Observed Gain5
Observed Loss6
Observed Complex0
Frequencyn/a


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