A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757146



Internal ID20533006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26527116..26527116hg38UCSC Ensembl
chr14:26996322..26996322hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277222
Samples
Known GenesNOVA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757146
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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