A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512438



Internal ID15851863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:51013394..51016130hg38UCSC Ensembl
Outerchr16:51047305..51050041hg19UCSC Ensembl
Outerchr16:49604806..49607542hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg382737
hg192737
hg182737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625031
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)nsv512438
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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