A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512569



Internal ID15851994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21719645..21723112hg38UCSC Ensembl
Outerchr19:21902447..21905914hg19UCSC Ensembl
Outerchr19:21694287..21697754hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg383468
hg193468
hg183468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625178
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)nsv512569
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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