A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19665



Internal ID15834886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60126..87161hg38UCSC Ensembl
Outerchr11:60001..87567hg38UCSC Ensembl
Innerchr11:60126..87161hg19UCSC Ensembl
Outerchr11:60001..87567hg19UCSC Ensembl
Innerchr11:50126..77161hg18UCSC Ensembl
Outerchr11:50001..77567hg18UCSC Ensembl
Innerchr11:50126..77161hg17UCSC Ensembl
Outerchr11:43965..77567hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3827567
hg1927567
hg1827567
hg1733603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8753
Supporting Variants
SamplesNA18537
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)nssv19665
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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