A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756307



Internal ID20532167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107476043..107476043hg38UCSC Ensembl
chr5:106811744..106811744hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271999
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756307
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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