A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018583



Internal ID22080214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54238851..54249648hg38UCSC Ensembl
Outerchr6:54230467..54253678hg38UCSC Ensembl
Innerchr6:54103649..54114446hg19UCSC Ensembl
Outerchr6:54095265..54118476hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3823212
hg1923212
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156503
Supporting Variants
Samples
Known GenesMLIP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018583
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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