A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761343



Internal ID20537203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35260216..35260216hg38UCSC Ensembl
chr1:35725817..35725817hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761343
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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