A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968485



Internal ID22743420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79560504..79560504hg38UCSC Ensembl
chr14:80026847..80026847hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385431
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968485
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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