A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155433



Internal ID22085938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38727277..38728719hg38UCSC Ensembl
Outerchr2:38721006..38729805hg38UCSC Ensembl
Innerchr2:38954419..38955861hg19UCSC Ensembl
Outerchr2:38948148..38956947hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011199
Samples
Known GenesGALM
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155433
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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