A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26531



Internal ID15497675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79706852..79714685hg38UCSC Ensembl
Outerchr17:79706133..79718128hg38UCSC Ensembl
Innerchr17:77680661..77688447hg19UCSC Ensembl
Outerchr17:77679942..77691895hg19UCSC Ensembl
Innerchr17:75295256..75303042hg18UCSC Ensembl
Outerchr17:75294537..75306490hg18UCSC Ensembl
Innerchr17:75295256..75303042hg17UCSC Ensembl
Outerchr17:75294537..75306490hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811996
hg1911954
hg1811954
hg1711954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9594
Supporting Variants
SamplesNA19240
Known GenesMIR4739
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)nssv26531
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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