A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22581



Internal ID15491687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45928987..45929024hg38UCSC Ensembl
Outerchr10:45928396..45929593hg38UCSC Ensembl
Innerchr10:51327898..51327935hg19UCSC Ensembl
Outerchr10:51327307..51328504hg19UCSC Ensembl
Innerchr10:50997904..50997941hg18UCSC Ensembl
Outerchr10:50997313..50998510hg18UCSC Ensembl
Innerchr10:50997904..50997941hg17UCSC Ensembl
Outerchr10:50997313..50998510hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381198
hg191198
hg181198
hg171198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8647
Supporting Variants
SamplesNA18860
Known GenesLOC728407, PARG
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)nssv22581
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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