A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034583



Internal ID21943926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42813066..42813126hg38UCSC Ensembl
chr17:40965084..40965144hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627960
Samples
Known GenesBECN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034583
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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