A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105749



Internal ID21275512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141580507..141659516hg38UCSC Ensembl
Innerchr2:142338076..142417085hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3879010
hg1979010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111413
Supporting Variants
Samplessample223
Known GenesLRP1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105749
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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