A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060398



Internal ID21969631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41930007..41933376hg38UCSC Ensembl
chr21:43350116..43353485hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383370
hg193370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646926
Samples
Known GenesC2CD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060398
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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