A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511920



Internal ID15504659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158126661..158128088hg38UCSC Ensembl
Outerchr6:158547693..158549120hg19UCSC Ensembl
Outerchr6:158467681..158469108hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381428
hg191428
hg181428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624457
Samples1
Known GenesSERAC1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511920
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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