A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757686



Internal ID20533546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161035887..161035887hg38UCSC Ensembl
chr1:161005677..161005677hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757686
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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