A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609265



Internal ID21801312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78279677..78281228hg38UCSC Ensembl
chr14:78746020..78747571hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038334
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609265
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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