A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145916



Internal ID345121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79753637..79773713hg38UCSC Ensembl
chr14:80219980..80240056hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3820077
hg1920077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698947
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145916
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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