A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156503



Internal ID22086904
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018584, nssv4018583, nssv4018585
Samples
Known GenesMLIP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156503
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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