A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155975



Internal ID22086480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74834930..75420342hg38UCSC Ensembl
Outerchr3:74831014..75434094hg38UCSC Ensembl
Innerchr3:74884081..75469493hg19UCSC Ensembl
Outerchr3:74880165..75483245hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38603081
hg19603081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016408
Samples
Known GenesFAM86DP, MIR4444-1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155975
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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