A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029134



Internal ID21938477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64368998..64369170hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029134
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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