A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155889



Internal ID22086394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:181865856..181956923hg38UCSC Ensembl
Outerchr2:181860571..181970084hg38UCSC Ensembl
Innerchr2:182730583..182821650hg19UCSC Ensembl
Outerchr2:182725298..182834811hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38109514
hg19109514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016115
Samples
Known GenesPPP1R1C, SSFA2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155889
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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