A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265332



Internal ID20474550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235525583..235525886hg38UCSC Ensembl
chr2:236434227..236434530hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745489
Supporting Variants
Samples
Known GenesAGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265332
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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