A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114443



Internal ID21297709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27444473..27465853hg38UCSC Ensembl
Innerchr1:27770986..27792364hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3821381
hg1921379
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098580
Samplessample375
Known GenesWASF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114443
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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