A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512137



Internal ID15504876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1409216..1411053hg38UCSC Ensembl
Outerchr10:1451411..1453248hg19UCSC Ensembl
Outerchr10:1441411..1443248hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381838
hg191838
hg181838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624697
Samples1
Known GenesADARB2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512137
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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