A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953886



Internal ID21373955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143801119..143801271hg38UCSC Ensembl
chr2:144558688..144558840hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178377
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953886
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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