A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764392



Internal ID20540252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59406196..59406196hg38UCSC Ensembl
chr1:59871868..59871868hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292948
Samples
Known GenesFGGY
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764392
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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