A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19021



Internal ID15844514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:320139..322407hg38UCSC Ensembl
Outerchr9:319952..322740hg38UCSC Ensembl
Innerchr9:320139..322407hg19UCSC Ensembl
Outerchr9:319952..322740hg19UCSC Ensembl
Innerchr9:310139..312407hg18UCSC Ensembl
Outerchr9:309952..312740hg18UCSC Ensembl
Innerchr9:310139..312407hg17UCSC Ensembl
Outerchr9:309952..312740hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg382789
hg192789
hg182789
hg172789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8403
Supporting Variants
SamplesNA19240
Known GenesDOCK8
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)nssv19021
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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