A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733698



Internal ID20509628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170621443..170624527hg38UCSC Ensembl
chr2:171477953..171481037hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285389
Samples
Known GenesMYO3B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733698
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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