A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645780



Internal ID21837827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17408743..17528852hg38UCSC Ensembl
chr21:18781062..18901170hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38120110
hg19120109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057049
Supporting Variants
Samples
Known GenesC21orf37, CXADR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645780
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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