A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18865



Internal ID15840826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48881460..48909209hg19UCSC Ensembl
Outerchr10:48880944..48910778hg19UCSC Ensembl
Innerchr10:48501466..48529215hg18UCSC Ensembl
Outerchr10:48500950..48530784hg18UCSC Ensembl
Innerchr10:48501466..48529215hg17UCSC Ensembl
Outerchr10:48500950..48530784hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1929835
hg1829835
hg1729835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18980
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)nssv18865
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer