A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25348



Internal ID15488141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35307410..35313812hg38UCSC Ensembl
Outerchr19:35306287..35314293hg38UCSC Ensembl
Innerchr19:35798313..35804715hg19UCSC Ensembl
Outerchr19:35797190..35805196hg19UCSC Ensembl
Innerchr19:40490153..40496555hg18UCSC Ensembl
Outerchr19:40489030..40497036hg18UCSC Ensembl
Innerchr19:40490153..40496555hg17UCSC Ensembl
Outerchr19:40489030..40497036hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg388007
hg198007
hg188007
hg178007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9711
Supporting Variants
SamplesNA18537
Known GenesMAG
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)nssv25348
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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