A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19981



Internal ID15497932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61872914..61873898hg38UCSC Ensembl
Outerchr9:61872513..61874131hg38UCSC Ensembl
Innerchr9:46130844..46131828hg19UCSC Ensembl
Outerchr9:46130443..46132061hg19UCSC Ensembl
Innerchr9:46020840..46021824hg18UCSC Ensembl
Outerchr9:46020439..46022057hg18UCSC Ensembl
Innerchr9:44683589..44684573hg17UCSC Ensembl
Outerchr9:44683188..44684806hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381619
hg191619
hg181619
hg171619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8474
Supporting Variants
SamplesNA19240
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)nssv19981
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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