A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22662



Internal ID15486107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61160696..61169687hg38UCSC Ensembl
Outerchr11:61160262..61170195hg38UCSC Ensembl
Innerchr11:60928168..60937159hg19UCSC Ensembl
Outerchr11:60927734..60937667hg19UCSC Ensembl
Innerchr11:60684744..60693735hg18UCSC Ensembl
Outerchr11:60684310..60694243hg18UCSC Ensembl
Innerchr11:60684744..60693735hg17UCSC Ensembl
Outerchr11:60684310..60694243hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg389934
hg199934
hg189934
hg179934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8832
Supporting Variants
SamplesNA18502
Known GenesVPS37C
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)nssv22662
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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