A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21813



Internal ID15828252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43845955..43848403hg38UCSC Ensembl
Outerchr15:43843954..43849428hg38UCSC Ensembl
Innerchr15:44138153..44140601hg19UCSC Ensembl
Outerchr15:44136152..44141626hg19UCSC Ensembl
Innerchr15:41925445..41927893hg18UCSC Ensembl
Outerchr15:41923444..41928918hg18UCSC Ensembl
Innerchr15:41925445..41927893hg17UCSC Ensembl
Outerchr15:41923444..41928918hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg385475
hg195475
hg185475
hg175475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9255
Supporting Variants
SamplesNA07048
Known GenesWDR76
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)nssv21813
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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