A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20157



Internal ID15842093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33617696..33618422hg38UCSC Ensembl
Outerchr9:33617285..33618943hg38UCSC Ensembl
Innerchr9:33617694..33618420hg19UCSC Ensembl
Outerchr9:33617283..33618941hg19UCSC Ensembl
Innerchr9:33607694..33608420hg18UCSC Ensembl
Outerchr9:33607283..33608941hg18UCSC Ensembl
Innerchr9:33607694..33608420hg17UCSC Ensembl
Outerchr9:33607283..33608941hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381659
hg191659
hg181659
hg171659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8441
Supporting Variants
SamplesNA19132
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)nssv20157
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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