A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511907



Internal ID15851332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:99586587..99587639hg38UCSC Ensembl
Outerchr6:100034463..100035515hg19UCSC Ensembl
Outerchr6:100141184..100142236hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381053
hg191053
hg181053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624442
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)nsv511907
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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