A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26058



Internal ID15487203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19149405..19234553hg38UCSC Ensembl
Outerchr17:19148547..19235958hg38UCSC Ensembl
Innerchr17:19052718..19137866hg19UCSC Ensembl
Outerchr17:19051860..19139271hg19UCSC Ensembl
Innerchr17:18993443..19078459hg18UCSC Ensembl
Outerchr17:18992585..19079864hg18UCSC Ensembl
Innerchr17:18993443..19078459hg17UCSC Ensembl
Outerchr17:18992585..19079864hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3887412
hg1987412
hg1887280
hg1787280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9504
Supporting Variants
SamplesNA18504
Known GenesGRAPL
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)nssv26058
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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