A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483386



Internal ID22541293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235835190..235861442hg38UCSC Ensembl
chr2:236743834..236770086hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3826253
hg1926253
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832254
Supporting Variants
Samples
Known GenesAGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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