A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533355



Internal ID21857711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:49955329..49964958hg38UCSC Ensembl
chr2:50182467..50192096hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg389630
hg199630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989442
Supporting Variants
Samples
Known GenesNRXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533355
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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