A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22590



Internal ID15843798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41359500..41359842hg38UCSC Ensembl
Outerchr9:41351993..41360525hg38UCSC Ensembl
Innerchr9:45442523..45442865hg19UCSC Ensembl
Outerchr9:45435016..45443548hg19UCSC Ensembl
Innerchr9:45332519..45332861hg18UCSC Ensembl
Outerchr9:45325012..45333544hg18UCSC Ensembl
Innerchr9:44381459..44381801hg17UCSC Ensembl
Outerchr9:44373952..44382484hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388533
hg198533
hg188533
hg178533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8472
Supporting Variants
SamplesNA19221
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)nssv22590
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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