A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755939



Internal ID20531799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28247126..28247126hg38UCSC Ensembl
chr1:28573637..28573637hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755939
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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