A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753077



Internal ID20528937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92846790..92846790hg38UCSC Ensembl
chr1:93312347..93312347hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275008
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753077
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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