A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9663



Internal ID15500889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1400724..1403362hg38UCSC Ensembl
Outerchr19:1400723..1403361hg19UCSC Ensembl
Outerchr19:1351723..1354361hg18UCSC Ensembl
Outerchr19:1351723..1354361hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382639
hg192639
hg182639
hg172639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24740, nssv24055, nssv24855
SamplesNA18975, NA10839, NA18564
Known GenesGAMT
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)nsv9663
Frequency
Sample Size31
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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