A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014242



Internal ID22075873
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156150
Supporting Variants
Samples
Known GenesATP8A1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014242
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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