A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19180



Internal ID15831881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20995051..20995399hg38UCSC Ensembl
Outerchr15:20992779..20996708hg38UCSC Ensembl
Innerchr15:21200380..21200728hg19UCSC Ensembl
Outerchr15:21198108..21202037hg19UCSC Ensembl
Innerchr15:19465039..19465387hg18UCSC Ensembl
Outerchr15:19462767..19466696hg18UCSC Ensembl
Innerchr15:19465039..19465387hg17UCSC Ensembl
Outerchr15:19462767..19466696hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383930
hg193930
hg183930
hg173930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12802
Known GenesCT60
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)nssv19180
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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