A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755641



Internal ID20531501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79921784..79921784hg38UCSC Ensembl
chr14:80388127..80388127hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755641
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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