A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642780



Internal ID21834827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9988466..9997711hg38UCSC Ensembl
chr21:10466494..10475739hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg389246
hg199246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642780
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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