A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745582



Internal ID20521592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14902958..14903040hg38UCSC Ensembl
chr21:16275279..16275361hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745582
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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