A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156150



Internal ID22086655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42596221..42646167hg38UCSC Ensembl
Outerchr4:42592928..42646298hg38UCSC Ensembl
Innerchr4:42598238..42648184hg19UCSC Ensembl
Outerchr4:42594945..42648315hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3853371
hg1953371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014242
Samples
Known GenesATP8A1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156150
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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