A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639029



Internal ID21831076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:24661942..24676630hg38UCSC Ensembl
chr21:26034256..26048944hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3814689
hg1914689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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