A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19337



Internal ID15835908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48105976..48283411hg19UCSC Ensembl
Innerchr10:47725982..47903417hg18UCSC Ensembl
Innerchr10:47725982..47903417hg17UCSC Ensembl
Outerchr10:47575187..47904383hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19177436
hg18177436
hg17329197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18563
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, CTSLP2, FAM25C, FAM25G
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)nssv19337
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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