A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749984



Internal ID20526019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38815941..38815997hg38UCSC Ensembl
chr21:40187865..40187921hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265465
Samples
Known GenesETS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749984
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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