A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759685



Internal ID20535546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91836575..91836575hg38UCSC Ensembl
chr14:92302919..92302919hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276163
Samples
Known GenesTC2N
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759685
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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