A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512581



Internal ID15505320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35288658..35290659hg38UCSC Ensembl
Outerchr19:35779561..35781562hg19UCSC Ensembl
Outerchr19:40471401..40473402hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382002
hg192002
hg182002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625191
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)nsv512581
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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