A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24193



Internal ID15843894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50659898..50701302hg38UCSC Ensembl
Outerchr10:50658126..50701319hg38UCSC Ensembl
Innerchr10:52419658..52461062hg19UCSC Ensembl
Outerchr10:52417886..52461079hg19UCSC Ensembl
Innerchr10:52089664..52131068hg18UCSC Ensembl
Outerchr10:52087892..52131085hg18UCSC Ensembl
Innerchr10:52089664..52131068hg17UCSC Ensembl
Outerchr10:52087892..52131085hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3843194
hg1943194
hg1843194
hg1743194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8662
Supporting Variants
SamplesNA19221
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)nssv24193
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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