A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752781



Internal ID20528641
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 StatusM
Merged Variants
Supporting Variantsnssv16260684
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752781
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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