A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765897



Internal ID20541757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110120474..110120474hg38UCSC Ensembl
chr1:110663096..110663096hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382741
hg192741
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765897
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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