A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759582



Internal ID20535442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84756748..84756748hg38UCSC Ensembl
chr1:85222431..85222431hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759582
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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