A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029541



Internal ID21938884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80401623..80403995hg38UCSC Ensembl
chr17:78375423..78377795hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636270
Samples
Known GenesLOC100294362
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029541
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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