A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756357



Internal ID20532217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97787740..97787740hg38UCSC Ensembl
chr14:98254077..98254077hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756357
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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