A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155897



Internal ID22086402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:188400660..188664764hg38UCSC Ensembl
Outerchr2:188390524..188667452hg38UCSC Ensembl
Innerchr2:189265387..189529491hg19UCSC Ensembl
Outerchr2:189255251..189532179hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38276929
hg19276929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016128
Samples
Known GenesGULP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155897
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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