A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044085



Internal ID21953376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29058190..29058319hg38UCSC Ensembl
chr21:30430511..30430640hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638311
Samples
Known GenesCCT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044085
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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