A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9704



Internal ID15847616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29127456..29140649hg38UCSC Ensembl
Outerchr19:29618363..29631556hg19UCSC Ensembl
Outerchr19:34310203..34323396hg18UCSC Ensembl
Outerchr19:34310203..34323396hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3813194
hg1913194
hg1813194
hg1713194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24764
SamplesNA18552
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)nsv9704
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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