A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25603



Internal ID15495724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60099093..60110531hg38UCSC Ensembl
Outerchr17:60090914..60112285hg38UCSC Ensembl
Innerchr17:58176454..58187892hg19UCSC Ensembl
Outerchr17:58168275..58189646hg19UCSC Ensembl
Innerchr17:55531236..55542674hg18UCSC Ensembl
Outerchr17:55523057..55544428hg18UCSC Ensembl
Innerchr17:55531236..55542674hg17UCSC Ensembl
Outerchr17:55523057..55544428hg17UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg3821372
hg1921372
hg1821372
hg1721372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9579
Supporting Variants
SamplesNA19144
Known GenesLOC653653
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)nssv25603
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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