A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057049



Internal ID21966285
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 StatusM
Merged Variants
Supporting Variantsnssv17645780
Samples
Known GenesC21orf37, CXADR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057049
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer