A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25121



Internal ID15489784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35371098..35371278hg38UCSC Ensembl
Outerchr19:35370611..35371933hg38UCSC Ensembl
Innerchr19:35862000..35862180hg19UCSC Ensembl
Outerchr19:35861513..35862835hg19UCSC Ensembl
Innerchr19:40553840..40554020hg18UCSC Ensembl
Outerchr19:40553353..40554675hg18UCSC Ensembl
Innerchr19:40553840..40554020hg17UCSC Ensembl
Outerchr19:40553353..40554675hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381323
hg191323
hg181323
hg171323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9712
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)nssv25121
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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