A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512896



Internal ID15852318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:137117234..137117620hg38UCSC Ensembl
Outerchr6:137438371..137438757hg19UCSC Ensembl
Outerchr6:137480064..137480450hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38871
hg19871
hg18871
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625541
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)nsv512896
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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