A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10807



Internal ID15499084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29530551..29533562hg38UCSC Ensembl
Outerchr6:29498328..29501339hg19UCSC Ensembl
Outerchr6:29606307..29609318hg18UCSC Ensembl
Outerchr6:29606307..29609318hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383012
hg193012
hg183012
hg173012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13492, nssv14676
SamplesNA10863, NA18942
Known GenesLINC01015
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)nsv10807
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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