A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641135



Internal ID21833182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29058689..29058786hg38UCSC Ensembl
chr21:30431010..30431107hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042402
Supporting Variants
Samples
Known GenesCCT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641135
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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