A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512900



Internal ID15852322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166030515..166031261hg38UCSC Ensembl
Outerchr6:166444003..166444749hg19UCSC Ensembl
Outerchr6:166363993..166364739hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381406
hg191406
hg181406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625546
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)nsv512900
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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