A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765308



Internal ID20541168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111697499..111697499hg38UCSC Ensembl
chr6:112018702..112018702hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270915
Samples
Known GenesFYN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765308
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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