A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051193



Internal ID21960426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43743329..43743426hg38UCSC Ensembl
chr21:45163210..45163307hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639121
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051193
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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