A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756273



Internal ID20532133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21858055..21858055hg38UCSC Ensembl
chr14:22326232..22326232hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756273
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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