A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19913



Internal ID15492780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15008250..15008872hg38UCSC Ensembl
Outerchr8:15007415..15009750hg38UCSC Ensembl
Innerchr8:14865759..14866381hg19UCSC Ensembl
Outerchr8:14864924..14867259hg19UCSC Ensembl
Innerchr8:14910130..14910752hg18UCSC Ensembl
Outerchr8:14909295..14911630hg18UCSC Ensembl
Innerchr8:14910130..14910752hg17UCSC Ensembl
Outerchr8:14909295..14911630hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382336
hg192336
hg182336
hg172336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8298
Supporting Variants
SamplesNA18972
Known GenesSGCZ
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)nssv19913
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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