A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26417



Internal ID15844399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60025526..60027025hg38UCSC Ensembl
Outerchr17:60024228..60028285hg38UCSC Ensembl
Innerchr17:58102887..58104386hg19UCSC Ensembl
Outerchr17:58101589..58105646hg19UCSC Ensembl
Innerchr17:55457669..55459168hg18UCSC Ensembl
Outerchr17:55456371..55460428hg18UCSC Ensembl
Innerchr17:55457669..55459168hg17UCSC Ensembl
Outerchr17:55456371..55460428hg17UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg384058
hg194058
hg184058
hg174058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9578
Supporting Variants
SamplesNA19240
Known Genes
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)nssv26417
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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