A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765419



Internal ID20541279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106859886..106859886hg38UCSC Ensembl
chr6:107307762..107307762hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765419
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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