A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21708



Internal ID15836578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21073452..21076905hg38UCSC Ensembl
Outerchr15:21072875..21077635hg38UCSC Ensembl
Innerchr15:21278781..21282234hg19UCSC Ensembl
Outerchr15:21278204..21282964hg19UCSC Ensembl
Innerchr15:19543440..19546893hg18UCSC Ensembl
Outerchr15:19542863..19547623hg18UCSC Ensembl
Innerchr15:19543440..19546893hg17UCSC Ensembl
Outerchr15:19542863..19547623hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384761
hg194761
hg184761
hg174761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18564
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)nssv21708
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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