A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511686



Internal ID15851111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:27852703..27855519hg38UCSC Ensembl
Outerchr1:28179214..28182030hg19UCSC Ensembl
Outerchr1:28051801..28054617hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382817
hg192817
hg182817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626325
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511686
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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