A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19597



Internal ID15830104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46843083..46862128hg38UCSC Ensembl
Outerchr10:46841978..46868354hg38UCSC Ensembl
Innerchr10:48877234..48896279hg19UCSC Ensembl
Outerchr10:48871008..48897384hg19UCSC Ensembl
Innerchr10:48497240..48516285hg18UCSC Ensembl
Outerchr10:48491014..48517390hg18UCSC Ensembl
Innerchr10:48497240..48516285hg17UCSC Ensembl
Outerchr10:48491014..48517390hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3826377
hg1926377
hg1826377
hg1726377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA11830
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)nssv19597
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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