A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278065



Internal ID20487283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79966899..79972946hg38UCSC Ensembl
chr4:80888053..80894100hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg386048
hg196048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741338
Supporting Variants
Samples
Known GenesANTXR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278065
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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