A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744025



Internal ID20520019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214596756..214597091hg38UCSC Ensembl
chr1:214770099..214770434hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744025
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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