A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17898



Internal ID15836600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7444425..7445034hg38UCSC Ensembl
Outerchr9:7443283..7446270hg38UCSC Ensembl
Innerchr9:7444425..7445034hg19UCSC Ensembl
Outerchr9:7443283..7446270hg19UCSC Ensembl
Innerchr9:7434425..7435034hg18UCSC Ensembl
Outerchr9:7433283..7436270hg18UCSC Ensembl
Innerchr9:7434425..7435034hg17UCSC Ensembl
Outerchr9:7433283..7436270hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382988
hg192988
hg182988
hg172988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8411
Supporting Variants
SamplesNA18564
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)nssv17898
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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