A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260684



Internal ID20469902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24926976..24926976hg38UCSC Ensembl
chr6:24927204..24927204hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752781
Supporting Variants
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260684
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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