A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986429



Internal ID21895772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149213267..149213342hg38UCSC Ensembl
chr2:150069781..150069856hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536209
Samples
Known GenesLYPD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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