A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739807



Internal ID20515783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92215792..92215845hg38UCSC Ensembl
chr1:92681349..92681402hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739807
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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