A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056842



Internal ID21966077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39974383..39975151hg38UCSC Ensembl
chr21:41346310..41347078hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056842
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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